x0.body_genetic

31 forms

Name

Type

Description | Question | Decode (Coded Value)

Data type

Alias

x0.body_genetic

Item Group

Item Group x0.body_genetic

genetic_01

Item

Diabetes (Diabetes Mellitus)

integer

genetic_01 (VAR_NAMES)
Diabetes (Diabetes Mellitus) (LABEL)
integer (DATA_TYPE)
1=yes|0=no|999=not stated (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
940 (VARIABLE_ORDER)
Zuckerkrankheit (Diabetes mellitus) (LABEL_DE)
1=ja|0=nein|999=keine Angabe (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_01 (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.123

Code List

Diabetes (Diabetes Mellitus)

CL Item

yes (1)

CL Item

no (0)

CL Item

not stated (999)

genetic_01a

Item

Diabetes (Diabetes Mellitus) (Father)

integer

genetic_01a (VAR_NAMES)
Diabetes (Diabetes Mellitus) (Father) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
950 (VARIABLE_ORDER)
Zuckerkrankheit (Diabetes mellitus) [Vater] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_01a (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Diabetes (Diabetes Mellitus) (Father)

CL Item

yes (1)

CL Item

no (0)

genetic_01b

Item

Diabetes (Diabetes Mellitus) (Mother)

integer

genetic_01b (VAR_NAMES)
Diabetes (Diabetes Mellitus) (Mother) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
960 (VARIABLE_ORDER)
Zuckerkrankheit (Diabetes mellitus) [Mutter] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_01b (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Diabetes (Diabetes Mellitus) (Mother)

CL Item

yes (1)

CL Item

no (0)

genetic_01c

Item

Diabetes (Diabetes Mellitus) (Siblings)

integer

genetic_01c (VAR_NAMES)
Diabetes (Diabetes Mellitus) (Siblings) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
970 (VARIABLE_ORDER)
Zuckerkrankheit (Diabetes mellitus) [Geschwister] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_01c (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Diabetes (Diabetes Mellitus) (Siblings)

CL Item

yes (1)

CL Item

no (0)

genetic_01d

Item

Diabetes (Diabetes Mellitus) (Children)

integer

genetic_01d (VAR_NAMES)
Diabetes (Diabetes Mellitus) (Children) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
980 (VARIABLE_ORDER)
Zuckerkrankheit (Diabetes mellitus) [Kinder] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_01d (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Diabetes (Diabetes Mellitus) (Children)

CL Item

yes (1)

CL Item

no (0)

genetic_01e

Item

Diabetes (Diabetes Mellitus) (Not Specified)

integer

genetic_01e (VAR_NAMES)
Diabetes (Diabetes Mellitus) (Not Specified) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
990 (VARIABLE_ORDER)
Zuckerkrankheit (Diabetes mellitus) [keine Angabe] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_01e (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Diabetes (Diabetes Mellitus) (Not Specified)

CL Item

yes (1)

CL Item

no (0)

genetic_02

Item

High Blood Pressure

integer

genetic_02 (VAR_NAMES)
High Blood Pressure (LABEL)
integer (DATA_TYPE)
1=yes|0=no|999=not stated (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1000 (VARIABLE_ORDER)
Hoher Blutdruck (LABEL_DE)
1=ja|0=nein|999=keine Angabe (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_02 (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.123

Code List

High Blood Pressure

CL Item

yes (1)

CL Item

no (0)

CL Item

not stated (999)

genetic_02a

Item

High Blood Pressure (Father)

integer

genetic_02a (VAR_NAMES)
High Blood Pressure (Father) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1010 (VARIABLE_ORDER)
Hoher Blutdruck [Vater] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_02a (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

High Blood Pressure (Father)

CL Item

yes (1)

CL Item

no (0)

genetic_02b

Item

High Blood Pressure (Mother)

integer

genetic_02b (VAR_NAMES)
High Blood Pressure (Mother) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1020 (VARIABLE_ORDER)
Hoher Blutdruck [Mutter] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_02b (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

High Blood Pressure (Mother)

CL Item

yes (1)

CL Item

no (0)

genetic_02c

Item

High Blood Pressure (Siblings)

integer

genetic_02c (VAR_NAMES)
High Blood Pressure (Siblings) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1030 (VARIABLE_ORDER)
Hoher Blutdruck [Geschwister] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_02c (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

High Blood Pressure (Siblings)

CL Item

yes (1)

CL Item

no (0)

genetic_02d

Item

High Blood Pressure (Children)

integer

genetic_02d (VAR_NAMES)
High Blood Pressure (Children) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1040 (VARIABLE_ORDER)
Hoher Blutdruck [Kinder] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_02d (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

High Blood Pressure (Children)

CL Item

yes (1)

CL Item

no (0)

genetic_02e

Item

High Blood Pressure (Not Specified)

integer

genetic_02e (VAR_NAMES)
High Blood Pressure (Not Specified) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1050 (VARIABLE_ORDER)
Hoher Blutdruck [keine Angabe] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_02e (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

High Blood Pressure (Not Specified)

CL Item

yes (1)

CL Item

no (0)

genetic_03

Item

Heart Attack

integer

genetic_03 (VAR_NAMES)
Heart Attack (LABEL)
integer (DATA_TYPE)
1=yes|0=no|999=not stated (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1060 (VARIABLE_ORDER)
Herzinfarkt (LABEL_DE)
1=ja|0=nein|999=keine Angabe (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_03 (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.123

Code List

Heart Attack

CL Item

yes (1)

CL Item

no (0)

CL Item

not stated (999)

genetic_03a

Item

Heart Attack (Father)

integer

genetic_03a (VAR_NAMES)
Heart Attack (Father) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1070 (VARIABLE_ORDER)
Herzinfarkt [Vater] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_03a (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Heart Attack (Father)

CL Item

yes (1)

CL Item

no (0)

genetic_03b

Item

Heart Attack (Mother)

integer

genetic_03b (VAR_NAMES)
Heart Attack (Mother) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1080 (VARIABLE_ORDER)
Herzinfarkt [Mutter] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_03b (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Heart Attack (Mother)

CL Item

yes (1)

CL Item

no (0)

genetic_03c

Item

Heart Attack (Siblings)

integer

genetic_03c (VAR_NAMES)
Heart Attack (Siblings) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1090 (VARIABLE_ORDER)
Herzinfarkt [Geschwister] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_03c (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Heart Attack (Siblings)

CL Item

yes (1)

CL Item

no (0)

genetic_03d

Item

Heart Attack (Children)

integer

genetic_03d (VAR_NAMES)
Heart Attack (Children) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1100 (VARIABLE_ORDER)
Herzinfarkt [Kinder] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_03d (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Heart Attack (Children)

CL Item

yes (1)

CL Item

no (0)

genetic_03e

Item

Heart Attack (Not Specified)

integer

genetic_03e (VAR_NAMES)
Heart Attack (Not Specified) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1110 (VARIABLE_ORDER)
Herzinfarkt [keine Angabe] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_03e (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Heart Attack (Not Specified)

CL Item

yes (1)

CL Item

no (0)

genetic_04

Item

Stroke

integer

genetic_04 (VAR_NAMES)
Stroke (LABEL)
integer (DATA_TYPE)
1=yes|0=no|999=not stated (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1120 (VARIABLE_ORDER)
Schlaganfall (LABEL_DE)
1=ja|0=nein|999=keine Angabe (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_04 (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.123

Code List

Stroke

CL Item

yes (1)

CL Item

no (0)

CL Item

not stated (999)

genetic_04a

Item

Stroke (Father)

integer

genetic_04a (VAR_NAMES)
Stroke (Father) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1130 (VARIABLE_ORDER)
Schlaganfall [Vater] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_04a (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Stroke (Father)

CL Item

yes (1)

CL Item

no (0)

genetic_04b

Item

Stroke (Mother)

integer

genetic_04b (VAR_NAMES)
Stroke (Mother) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1140 (VARIABLE_ORDER)
Schlaganfall [Mutter] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_04b (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Stroke (Mother)

CL Item

yes (1)

CL Item

no (0)

genetic_04c

Item

Stroke (Sibling)

integer

genetic_04c (VAR_NAMES)
Stroke (Sibling) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1150 (VARIABLE_ORDER)
Schlaganfall [Geschwister] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_04c (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Stroke (Sibling)

CL Item

yes (1)

CL Item

no (0)

genetic_04d

Item

Stroke (Children)

integer

genetic_04d (VAR_NAMES)
Stroke (Children) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1160 (VARIABLE_ORDER)
Schlaganfall [Kinder] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_04d (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Stroke (Children)

CL Item

yes (1)

CL Item

no (0)

genetic_04e

Item

Stroke (Not Specified)

integer

genetic_04e (VAR_NAMES)
Stroke (Not Specified) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1170 (VARIABLE_ORDER)
Schlaganfall [keine Angabe] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_04e (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Stroke (Not Specified)

CL Item

yes (1)

CL Item

no (0)

genetic_05

Item

Asthma

integer

genetic_05 (VAR_NAMES)
Asthma (LABEL)
integer (DATA_TYPE)
1=yes|0=no|999=not stated (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1180 (VARIABLE_ORDER)
Asthma (LABEL_DE)
1=ja|0=nein|999=keine Angabe (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_05 (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.123

Code List

Asthma

CL Item

yes (1)

CL Item

no (0)

CL Item

not stated (999)

genetic_05a

Item

Asthma (Father)

integer

genetic_05a (VAR_NAMES)
Asthma (Father) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1190 (VARIABLE_ORDER)
Asthma [Vater] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_05a (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Asthma (Father)

CL Item

yes (1)

CL Item

no (0)

genetic_05b

Item

Asthma (Mother)

integer

genetic_05b (VAR_NAMES)
Asthma (Mother) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1200 (VARIABLE_ORDER)
Asthma [Mutter] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_05b (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Asthma (Mother)

CL Item

yes (1)

CL Item

no (0)

genetic_05c

Item

Asthma (Siblings)

integer

genetic_05c (VAR_NAMES)
Asthma (Siblings) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1210 (VARIABLE_ORDER)
Asthma [Geschwister] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_05c (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Asthma (Siblings)

CL Item

yes (1)

CL Item

no (0)

genetic_05d

Item

Asthma (Children)

integer

genetic_05d (VAR_NAMES)
Asthma (Children) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1220 (VARIABLE_ORDER)
Asthma [Kinder] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_05d (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Asthma (Children)

CL Item

yes (1)

CL Item

no (0)

genetic_05e

Item

Asthma (Not Specified)

integer

genetic_05e (VAR_NAMES)
Asthma (Not Specified) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1230 (VARIABLE_ORDER)
Asthma [keine Angabe] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_05e (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Asthma (Not Specified)

CL Item

yes (1)

CL Item

no (0)

genetic_06

Item

Blood Coagulation Disorders

integer

genetic_06 (VAR_NAMES)
Blood Coagulation Disorders (LABEL)
integer (DATA_TYPE)
1=yes|0=no|999=not stated (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1240 (VARIABLE_ORDER)
Blutgerinnungsstörungen, z. B. Bluter (LABEL_DE)
1=ja|0=nein|999=keine Angabe (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_06 (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.123

Code List

Blood Coagulation Disorders

CL Item

yes (1)

CL Item

no (0)

CL Item

not stated (999)

genetic_06a

Item

Blood Coagulation Disorders, e.g. Hemophiliacs (Father)

integer

genetic_06a (VAR_NAMES)
Blood Coagulation Disorders, e.g. Hemophiliacs (Father) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1250 (VARIABLE_ORDER)
Blutgerinnungsstörungen, z. B. Bluter [Vater] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_06a (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Blood Coagulation Disorders, e.g. Hemophiliacs (Father)

CL Item

yes (1)

CL Item

no (0)

genetic_06b

Item

Blood Coagulation Disorders, e.g. Hemophiliacs (Mother)

integer

genetic_06b (VAR_NAMES)
Blood Coagulation Disorders, e.g. Hemophiliacs (Mother) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1260 (VARIABLE_ORDER)
Blutgerinnungsstörungen, z. B. Bluter [Mutter] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_06b (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Blood Coagulation Disorders, e.g. Hemophiliacs (Mother)

CL Item

yes (1)

CL Item

no (0)

genetic_06c

Item

Blood Coagulation Disorders, e.g. Hemophiliacs (Siblings)

integer

genetic_06c (VAR_NAMES)
Blood Coagulation Disorders, e.g. Hemophiliacs (Siblings) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1270 (VARIABLE_ORDER)
Blutgerinnungsstörungen, z. B. Bluter [Geschwister] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_06c (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Blood Coagulation Disorders, e.g. Hemophiliacs (Siblings)

CL Item

yes (1)

CL Item

no (0)

genetic_06d

Item

Blood Coagulation Disorders, e.g. Hemophiliacs (Children)

integer

genetic_06d (VAR_NAMES)
Blood Coagulation Disorders, e.g. Hemophiliacs (Children) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1280 (VARIABLE_ORDER)
Blutgerinnungsstörungen, z. B. Bluter [Kinder] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_06d (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Blood Coagulation Disorders, e.g. Hemophiliacs (Children)

CL Item

yes (1)

CL Item

no (0)

genetic_06e

Item

Blood Coagulation Disorders, e.g. Hemophiliacs (Not Specified)

integer

genetic_06e (VAR_NAMES)
Blood Coagulation Disorders, e.g. Hemophiliacs (Not Specified) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1290 (VARIABLE_ORDER)
Blutgerinnungsstörungen, z. B. Bluter [keine Angabe] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_06e (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Blood Coagulation Disorders, e.g. Hemophiliacs (Not Specified)

CL Item

yes (1)

CL Item

no (0)

genetic_07

Item

Muscle Diseases, e.g. Muscle Weakness

integer

genetic_07 (VAR_NAMES)
Muscle Diseases, e.g. Muscle Weakness (LABEL)
integer (DATA_TYPE)
1=yes|0=no|999=not stated (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1300 (VARIABLE_ORDER)
Muskelerkrankungen, z. B. Muskelschwäche (LABEL_DE)
1=ja|0=nein|999=keine Angabe (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_07 (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.123

Code List

Muscle Diseases, e.g. Muscle Weakness

CL Item

yes (1)

CL Item

no (0)

CL Item

not stated (999)

genetic_07a

Item

Muscle Diseases, e.g. Muscle Weakness (Father)

integer

genetic_07a (VAR_NAMES)
Muscle Diseases, e.g. Muscle Weakness (Father) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1310 (VARIABLE_ORDER)
Muskelerkrankungen, z. B. Muskelschwäche [Vater] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_07a (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Muscle Diseases, e.g. Muscle Weakness (Father)

CL Item

yes (1)

CL Item

no (0)

genetic_07b

Item

Muscle Diseases, e.g. Muscle Weakness (Mother)

integer

genetic_07b (VAR_NAMES)
Muscle Diseases, e.g. Muscle Weakness (Mother) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1320 (VARIABLE_ORDER)
Muskelerkrankungen, z. B. Muskelschwäche [Mutter] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_07b (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Muscle Diseases, e.g. Muscle Weakness (Mother)

CL Item

yes (1)

CL Item

no (0)

genetic_07c

Item

Muscle Diseases, e.g. Muscle Weakness (Siblings)

integer

genetic_07c (VAR_NAMES)
Muscle Diseases, e.g. Muscle Weakness (Siblings) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1330 (VARIABLE_ORDER)
Muskelerkrankungen, z. B. Muskelschwäche [Geschwister] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_07c (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Muscle Diseases, e.g. Muscle Weakness (Siblings)

CL Item

yes (1)

CL Item

no (0)

genetic_07d

Item

Muscle Diseases, e.g. Muscle Weakness (Children)

integer

genetic_07d (VAR_NAMES)
Muscle Diseases, e.g. Muscle Weakness (Children) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1340 (VARIABLE_ORDER)
Muskelerkrankungen, z. B. Muskelschwäche [Kinder] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_07d (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Muscle Diseases, e.g. Muscle Weakness (Children)

CL Item

yes (1)

CL Item

no (0)

genetic_07e

Item

Muscle Diseases, e.g. Muscle Weakness (Not Specified)

integer

genetic_07e (VAR_NAMES)
Muscle Diseases, e.g. Muscle Weakness (Not Specified) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1350 (VARIABLE_ORDER)
Muskelerkrankungen, z. B. Muskelschwäche [keine Angabe] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_07e (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Muscle Diseases, e.g. Muscle Weakness (Not Specified)

CL Item

yes (1)

CL Item

no (0)

genetic_08

Item

Parkinson's Disease (Shaking Palsy)

integer

genetic_08 (VAR_NAMES)
Parkinson's Disease (Shaking Palsy) (LABEL)
integer (DATA_TYPE)
1=yes|0=no|999=not stated (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1360 (VARIABLE_ORDER)
Parkinson’sche Erkrankung (Schüttellähmung) (LABEL_DE)
1=ja|0=nein|999=keine Angabe (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_08 (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.123

Code List

Parkinson's Disease (Shaking Palsy)

CL Item

yes (1)

CL Item

no (0)

CL Item

not stated (999)

genetic_08a

Item

Parkinson's Disease (Shaking Palsy) (Father)

integer

genetic_08a (VAR_NAMES)
Parkinson's Disease (Shaking Palsy) (Father) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1370 (VARIABLE_ORDER)
Parkinson’sche Erkrankung (Schüttellähmung) [Vater] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_08a (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Parkinson's Disease (Shaking Palsy) (Father)

CL Item

yes (1)

CL Item

no (0)

genetic_08b

Item

Parkinson's Disease (Shaking Palsy) (Mother)

integer

genetic_08b (VAR_NAMES)
Parkinson's Disease (Shaking Palsy) (Mother) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1380 (VARIABLE_ORDER)
Parkinson’sche Erkrankung (Schüttellähmung) [Mutter] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_08b (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Parkinson's Disease (Shaking Palsy) (Mother)

CL Item

yes (1)

CL Item

no (0)

genetic_08c

Item

Parkinson's Disease (Shaking Palsy) (Sibling)

integer

genetic_08c (VAR_NAMES)
Parkinson's Disease (Shaking Palsy) (Sibling) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1390 (VARIABLE_ORDER)
Parkinson’sche Erkrankung (Schüttellähmung) [Geschwister] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_08c (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Parkinson's Disease (Shaking Palsy) (Sibling)

CL Item

yes (1)

CL Item

no (0)

genetic_08d

Item

Parkinson's Disease (Shaking Palsy) (Children)

integer

genetic_08d (VAR_NAMES)
Parkinson's Disease (Shaking Palsy) (Children) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1400 (VARIABLE_ORDER)
Parkinson’sche Erkrankung (Schüttellähmung) [Kinder] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_08d (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Parkinson's Disease (Shaking Palsy) (Children)

CL Item

yes (1)

CL Item

no (0)

genetic_08e

Item

Parkinson's Disease (Shaking Palsy) (Not Specified)

integer

genetic_08e (VAR_NAMES)
Parkinson's Disease (Shaking Palsy) (Not Specified) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1410 (VARIABLE_ORDER)
Parkinson’sche Erkrankung (Schüttellähmung) [keine Angabe] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_08e (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Parkinson's Disease (Shaking Palsy) (Not Specified)

CL Item

yes (1)

CL Item

no (0)

genetic_09

Item

Mental Deficiency, e.g. Alzheimer's Disease

integer

genetic_09 (VAR_NAMES)
Mental Deficiency, e.g. Alzheimer's Disease (LABEL)
integer (DATA_TYPE)
1=yes|0=no|999=not stated (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1420 (VARIABLE_ORDER)
Geistesschwäche, z. B. Alzheimer (LABEL_DE)
1=ja|0=nein|999=keine Angabe (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_09 (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.123

Code List

Mental Deficiency, e.g. Alzheimer's Disease

CL Item

yes (1)

CL Item

no (0)

CL Item

not stated (999)

genetic_09a

Item

Mental Deficiency, e.g. Alzheimer's Disease (Father)

integer

genetic_09a (VAR_NAMES)
Mental Deficiency, e.g. Alzheimer's Disease (Father) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1430 (VARIABLE_ORDER)
Geistesschwäche, z. B. Alzheimer [Vater] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_09a (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Mental Deficiency, e.g. Alzheimer's Disease (Father)

CL Item

yes (1)

CL Item

no (0)

genetic_09b

Item

Mental Deficiency, e.g. Alzheimer's Disease (Mother)

integer

genetic_09b (VAR_NAMES)
Mental Deficiency, e.g. Alzheimer's Disease (Mother) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1440 (VARIABLE_ORDER)
Geistesschwäche, z. B. Alzheimer [Mutter] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_09b (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Mental Deficiency, e.g. Alzheimer's Disease (Mother)

CL Item

yes (1)

CL Item

no (0)

genetic_09c

Item

Mental Deficiency, e.g. Alzheimer's Disease (Siblings)

integer

genetic_09c (VAR_NAMES)
Mental Deficiency, e.g. Alzheimer's Disease (Siblings) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1450 (VARIABLE_ORDER)
Geistesschwäche, z. B. Alzheimer [Geschwister] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_09c (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Mental Deficiency, e.g. Alzheimer's Disease (Siblings)

CL Item

yes (1)

CL Item

no (0)

genetic_09d

Item

Mental Deficiency, e.g. Alzheimer's Disease (Children)

integer

genetic_09d (VAR_NAMES)
Mental Deficiency, e.g. Alzheimer's Disease (Children) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1460 (VARIABLE_ORDER)
Geistesschwäche, z. B. Alzheimer [Kinder] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_09d (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Mental Deficiency, e.g. Alzheimer's Disease (Children)

CL Item

yes (1)

CL Item

no (0)

genetic_09e

Item

Mental Deficiency, e.g. Alzheimer's Disease (Not Specified)

integer

genetic_09e (VAR_NAMES)
Mental Deficiency, e.g. Alzheimer's Disease (Not Specified) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1470 (VARIABLE_ORDER)
Geistesschwäche, z. B. Alzheimer [keine Angabe] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_09e (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Mental Deficiency, e.g. Alzheimer's Disease (Not Specified)

CL Item

yes (1)

CL Item

no (0)

genetic_10

Item

Epilepsy, i.e. Seizure Disorder

integer

genetic_10 (VAR_NAMES)
Epilepsy, i.e. Seizure Disorder (LABEL)
integer (DATA_TYPE)
1=yes|0=no|999=not stated (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1480 (VARIABLE_ORDER)
Epilepsie, d. h. Anfallsleiden (LABEL_DE)
1=ja|0=nein|999=keine Angabe (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_10 (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.123

Code List

Epilepsy, i.e. Seizure Disorder

CL Item

yes (1)

CL Item

no (0)

CL Item

not stated (999)

genetic_10a

Item

Epilepsy, i.e. Seizure Disorder (Father)

integer

genetic_10a (VAR_NAMES)
Epilepsy, i.e. Seizure Disorder (Father) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1490 (VARIABLE_ORDER)
Epilepsie, d. h. Anfallsleiden [Vater] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_10a (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Epilepsy, i.e. Seizure Disorder (Father)

CL Item

yes (1)

CL Item

no (0)

genetic_10b

Item

Epilepsy, i.e. Seizure Disorder (Mother)

integer

genetic_10b (VAR_NAMES)
Epilepsy, i.e. Seizure Disorder (Mother) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1500 (VARIABLE_ORDER)
Epilepsie, d. h. Anfallsleiden [Mutter] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_10b (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Epilepsy, i.e. Seizure Disorder (Mother)

CL Item

yes (1)

CL Item

no (0)

genetic_10c

Item

Epilepsy, i.e. Seizure Disorder (Sibling)

integer

genetic_10c (VAR_NAMES)
Epilepsy, i.e. Seizure Disorder (Sibling) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1510 (VARIABLE_ORDER)
Epilepsie, d. h. Anfallsleiden [Geschwister] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_10c (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Epilepsy, i.e. Seizure Disorder (Sibling)

CL Item

yes (1)

CL Item

no (0)

genetic_10d

Item

Epilepsy, i.e. Seizure Disorder (Children)

integer

genetic_10d (VAR_NAMES)
Epilepsy, i.e. Seizure Disorder (Children) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1520 (VARIABLE_ORDER)
Epilepsie, d. h. Anfallsleiden [Kinder] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_10d (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Epilepsy, i.e. Seizure Disorder (Children)

CL Item

yes (1)

CL Item

no (0)

genetic_10e

Item

Epilepsy, i.e. Seizure Disorder (Not Specified)

integer

genetic_10e (VAR_NAMES)
Epilepsy, i.e. Seizure Disorder (Not Specified) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1530 (VARIABLE_ORDER)
Epilepsie, d. h. Anfallsleiden [keine Angabe] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_10e (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Epilepsy, i.e. Seizure Disorder (Not Specified)

CL Item

yes (1)

CL Item

no (0)

genetic_11

Item

Cancer

integer

genetic_11 (VAR_NAMES)
Cancer (LABEL)
integer (DATA_TYPE)
1=yes|0=no|999=not stated (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1540 (VARIABLE_ORDER)
Krebserkrankung (LABEL_DE)
1=ja|0=nein|999=keine Angabe (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_11 (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.123

Code List

Cancer

CL Item

yes (1)

CL Item

no (0)

CL Item

not stated (999)

genetic_11a

Item

Cancer (Father)

integer

genetic_11a (VAR_NAMES)
Cancer (Father) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1550 (VARIABLE_ORDER)
Krebserkrankung [Vater] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_11a (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Cancer (Father)

CL Item

yes (1)

CL Item

no (0)

genetic_11b

Item

Cancer (Mother)

integer

genetic_11b (VAR_NAMES)
Cancer (Mother) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1560 (VARIABLE_ORDER)
Krebserkrankung [Mutter] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_11b (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Cancer (Mother)

CL Item

yes (1)

CL Item

no (0)

genetic_11c

Item

Cancer (Sibling)

integer

genetic_11c (VAR_NAMES)
Cancer (Sibling) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1570 (VARIABLE_ORDER)
Krebserkrankung [Geschwister] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_11c (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Cancer (Sibling)

CL Item

yes (1)

CL Item

no (0)

genetic_11d

Item

Cancer (Children)

integer

genetic_11d (VAR_NAMES)
Cancer (Children) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1580 (VARIABLE_ORDER)
Krebserkrankung [Kinder] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_11d (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Cancer (Children)

CL Item

yes (1)

CL Item

no (0)

genetic_11e

Item

Cancer (Not Specified)

integer

genetic_11e (VAR_NAMES)
Cancer (Not Specified) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1590 (VARIABLE_ORDER)
Krebserkrankung [keine Angabe] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_11e (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Cancer (Not Specified)

CL Item

yes (1)

CL Item

no (0)

genetic_11a1

Item

Welche Krebserkrankung hat Ihr Vater?

string

genetic_11a1 (VAR_NAMES)
Welche Krebserkrankung hat Ihr Vater? (LABEL)
string (DATA_TYPE)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1600 (VARIABLE_ORDER)
Welche Krebserkrankung hat Ihr Vater? (LABEL_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_11a1 (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

genetic_11b1

Item

What cancer does your mother have?

string

genetic_11b1 (VAR_NAMES)
What cancer does your mother have? (LABEL)
string (DATA_TYPE)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1610 (VARIABLE_ORDER)
Welche Krebserkrankung hat Ihre Mutter? (LABEL_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_11b1 (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

genetic_11c1

Item

What cancer do your siblings have?

string

genetic_11c1 (VAR_NAMES)
What cancer do your siblings have? (LABEL)
string (DATA_TYPE)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1620 (VARIABLE_ORDER)
Welche Krebserkrankung haben Ihre Geschwister? (LABEL_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_11c1 (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

genetic_11d1

Item

What cancer do your children have?

string

genetic_11d1 (VAR_NAMES)
What cancer do your children have? (LABEL)
string (DATA_TYPE)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1630 (VARIABLE_ORDER)
Welche Krebserkrankung haben Ihre Kinder? (LABEL_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_11d1 (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

genetic_12

Item

Congenital Physical Malformations

integer

genetic_12 (VAR_NAMES)
Congenital Physical Malformations (LABEL)
integer (DATA_TYPE)
1=yes|0=no|999=not stated (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1640 (VARIABLE_ORDER)
Angeborene körperliche Fehlbildungen (LABEL_DE)
1=ja|0=nein|999=keine Angabe (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_12 (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.123

Code List

Congenital Physical Malformations

CL Item

yes (1)

CL Item

no (0)

CL Item

not stated (999)

genetic_12a

Item

Congenital Physical Malformations (Father)

integer

genetic_12a (VAR_NAMES)
Congenital Physical Malformations (Father) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1650 (VARIABLE_ORDER)
Angeborene körperliche Fehlbildungen [Vater] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_12a (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Congenital Physical Malformations (Father)

CL Item

yes (1)

CL Item

no (0)

genetic_12b

Item

Congenital Physical Malformations (Mother)

integer

genetic_12b (VAR_NAMES)
Congenital Physical Malformations (Mother) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1660 (VARIABLE_ORDER)
Angeborene körperliche Fehlbildungen [Mutter] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_12b (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Congenital Physical Malformations (Mother)

CL Item

yes (1)

CL Item

no (0)

genetic_12c

Item

Congenital Physical Malformations (Siblings)

integer

genetic_12c (VAR_NAMES)
Congenital Physical Malformations (Siblings) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1670 (VARIABLE_ORDER)
Angeborene körperliche Fehlbildungen [Geschwister] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_12c (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Congenital Physical Malformations (Siblings)

CL Item

yes (1)

CL Item

no (0)

genetic_12d

Item

Congenital Physical Malformations (Children)

integer

genetic_12d (VAR_NAMES)
Congenital Physical Malformations (Children) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1680 (VARIABLE_ORDER)
Angeborene körperliche Fehlbildungen [Kinder] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_12d (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Congenital Physical Malformations (Children)

CL Item

yes (1)

CL Item

no (0)

genetic_12e

Item

Congenital Physical Malformations (Not Specified)

integer

genetic_12e (VAR_NAMES)
Congenital Physical Malformations (Not Specified) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1690 (VARIABLE_ORDER)
Angeborene körperliche Fehlbildungen [keine Angabe] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_12e (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Congenital Physical Malformations (Not Specified)

CL Item

yes (1)

CL Item

no (0)

genetic_12a1

Item

What congenital physical malformation does your father have?

string

genetic_12a1 (VAR_NAMES)
What congenital physical malformation does your father have? (LABEL)
string (DATA_TYPE)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1700 (VARIABLE_ORDER)
Welche angeborene körperliche Fehlbildung hat Ihr Vater? (LABEL_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_12a1 (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

genetic_12b1

Item

What congenital physical malformation does your mother have?

string

genetic_12b1 (VAR_NAMES)
What congenital physical malformation does your mother have? (LABEL)
string (DATA_TYPE)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1710 (VARIABLE_ORDER)
Welche angeborene körperliche Fehlbildung hat Ihre Mutter? (LABEL_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_12b1 (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

genetic_12c1

Item

What congenital physical malformations do your siblings have?

string

genetic_12c1 (VAR_NAMES)
What congenital physical malformations do your siblings have? (LABEL)
string (DATA_TYPE)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1720 (VARIABLE_ORDER)
Welche angeborenen körperlichen Fehlbildungen haben Ihre Geschwister? (LABEL_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_12c1 (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

genetic_12d1

Item

What congenital physical malformations do your children have?

string

genetic_12d1 (VAR_NAMES)
What congenital physical malformations do your children have? (LABEL)
string (DATA_TYPE)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1730 (VARIABLE_ORDER)
Welche angeborenen körperlichen Fehlbildungen haben Ihre Kinder? (LABEL_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_12d1 (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

genetic_13

Item

Allergies

integer

genetic_13 (VAR_NAMES)
Allergies (LABEL)
integer (DATA_TYPE)
1=yes|0=no|999=not stated (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1740 (VARIABLE_ORDER)
Allergien (LABEL_DE)
1=ja|0=nein|999=keine Angabe (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_13 (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.123

Code List

Allergies

CL Item

yes (1)

CL Item

no (0)

CL Item

not stated (999)

genetic_13a

Item

Allergies (Father)

integer

genetic_13a (VAR_NAMES)
Allergies (Father) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1750 (VARIABLE_ORDER)
Allergien [Vater] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_13a (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Allergies (Father)

CL Item

yes (1)

CL Item

no (0)

genetic_13b

Item

Allergies (Mother)

integer

genetic_13b (VAR_NAMES)
Allergies (Mother) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1760 (VARIABLE_ORDER)
Allergien [Mutter] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_13b (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Allergies (Mother)

CL Item

yes (1)

CL Item

no (0)

genetic_13c

Item

Allergies (Siblings)

integer

genetic_13c (VAR_NAMES)
Allergies (Siblings) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1770 (VARIABLE_ORDER)
Allergien [Geschwister] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_13c (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Allergies (Siblings)

CL Item

yes (1)

CL Item

no (0)

genetic_13d

Item

Allergies (Children)

integer

genetic_13d (VAR_NAMES)
Allergies (Children) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1780 (VARIABLE_ORDER)
Allergien [Kinder] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_13d (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Allergies (Children)

CL Item

yes (1)

CL Item

no (0)

genetic_13e

Item

Allergies (Not Specified)

integer

genetic_13e (VAR_NAMES)
Allergies (Not Specified) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1790 (VARIABLE_ORDER)
Allergien [keine Angabe] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_13e (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Allergies (Not Specified)

CL Item

yes (1)

CL Item

no (0)

genetic_13a1

Item

What allergies does your father have?

string

genetic_13a1 (VAR_NAMES)
What allergies does your father have? (LABEL)
string (DATA_TYPE)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1800 (VARIABLE_ORDER)
Welche Allergien hat Ihr Vater? (LABEL_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_13a1 (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

genetic_13b1

Item

What allergies does your mother have?

string

genetic_13b1 (VAR_NAMES)
What allergies does your mother have? (LABEL)
string (DATA_TYPE)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1810 (VARIABLE_ORDER)
Welche Allergien hat Ihre Mutter? (LABEL_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_13b1 (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

genetic_13c1

Item

What allergies do your siblings have?

string

genetic_13c1 (VAR_NAMES)
What allergies do your siblings have? (LABEL)
string (DATA_TYPE)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1820 (VARIABLE_ORDER)
Welche Allergien haben Ihre Geschwister? (LABEL_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_13c1 (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

genetic_13d1

Item

What allergies do your children have?

string

genetic_13d1 (VAR_NAMES)
What allergies do your children have? (LABEL)
string (DATA_TYPE)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1830 (VARIABLE_ORDER)
Welche Allergien haben Ihre Kinder? (LABEL_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_13d1 (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

genetic_14

Item

Gallstone Disease

integer

genetic_14 (VAR_NAMES)
Gallstone Disease (LABEL)
integer (DATA_TYPE)
1=yes|0=no|999=not stated (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1840 (VARIABLE_ORDER)
Gallensteinleiden (LABEL_DE)
1=ja|0=nein|999=keine Angabe (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_14 (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.123

Code List

Gallstone Disease

CL Item

yes (1)

CL Item

no (0)

CL Item

not stated (999)

genetic_14a

Item

Gallstone Disease (Father)

integer

genetic_14a (VAR_NAMES)
Gallstone Disease (Father) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1850 (VARIABLE_ORDER)
Gallensteinleiden [Vater] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_14a (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Gallstone Disease (Father)

CL Item

yes (1)

CL Item

no (0)

genetic_14b

Item

Gallstone Disease (Mother)

integer

genetic_14b (VAR_NAMES)
Gallstone Disease (Mother) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1860 (VARIABLE_ORDER)
Gallensteinleiden [Mutter] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_14b (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Gallstone Disease (Mother)

CL Item

yes (1)

CL Item

no (0)

genetic_14c

Item

Gallstone Disease (Siblings)

integer

genetic_14c (VAR_NAMES)
Gallstone Disease (Siblings) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1870 (VARIABLE_ORDER)
Gallensteinleiden [Geschwister] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_14c (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Gallstone Disease (Siblings)

CL Item

yes (1)

CL Item

no (0)

genetic_14d

Item

Gallstone Disease (Children)

integer

genetic_14d (VAR_NAMES)
Gallstone Disease (Children) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1880 (VARIABLE_ORDER)
Gallensteinleiden [Kinder] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_14d (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Gallstone Disease (Children)

CL Item

yes (1)

CL Item

no (0)

genetic_14e

Item

Gallstone Disease (Not Specified)

integer

genetic_14e (VAR_NAMES)
Gallstone Disease (Not Specified) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1890 (VARIABLE_ORDER)
Gallensteinleiden [keine Angabe] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_14e (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Gallstone Disease (Not Specified)

CL Item

yes (1)

CL Item

no (0)

genetic_15

Item

Gout

integer

genetic_15 (VAR_NAMES)
Gout (LABEL)
integer (DATA_TYPE)
1=yes|0=no|999=not stated (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1900 (VARIABLE_ORDER)
Gicht (LABEL_DE)
1=ja|0=nein|999=keine Angabe (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_15 (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.123

Code List

Gout

CL Item

yes (1)

CL Item

no (0)

CL Item

not stated (999)

genetic_15a

Item

Gout (Father)

integer

genetic_15a (VAR_NAMES)
Gout (Father) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1910 (VARIABLE_ORDER)
Gicht [Vater] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_15a (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Gout (Father)

CL Item

yes (1)

CL Item

no (0)

genetic_15b

Item

Gout (Mother)

integer

genetic_15b (VAR_NAMES)
Gout (Mother) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1920 (VARIABLE_ORDER)
Gicht [Mutter] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_15b (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Gout (Mother)

CL Item

yes (1)

CL Item

no (0)

genetic_15c

Item

Gout (Sibling)

integer

genetic_15c (VAR_NAMES)
Gout (Sibling) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1930 (VARIABLE_ORDER)
Gicht [Geschwister] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_15c (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Gout (Sibling)

CL Item

yes (1)

CL Item

no (0)

genetic_15d

Item

Gout (Children)

integer

genetic_15d (VAR_NAMES)
Gout (Children) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1940 (VARIABLE_ORDER)
Gicht [Kinder] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_15d (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Gout (Children)

CL Item

yes (1)

CL Item

no (0)

genetic_15e

Item

Gout (Not Specified)

integer

genetic_15e (VAR_NAMES)
Gout (Not Specified) (LABEL)
integer (DATA_TYPE)
1=yes|0=no (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1950 (VARIABLE_ORDER)
Gicht [keine Angabe] (LABEL_DE)
1=ja|0=nein (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_15e (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.75

Code List

Gout (Not Specified)

CL Item

yes (1)

CL Item

no (0)

genetic_16

Item

How many biological siblings (not half-siblings) do you have or have had?

float

genetic_16 (VAR_NAMES)
How many biological siblings (not half-siblings) do you have or have had? (LABEL)
float (DATA_TYPE)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1960 (VARIABLE_ORDER)
Wie viele leibliche Geschwister (keine Halbgeschwister) haben oder hatten Sie? (LABEL_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_16 (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

genetic_17

Item

Do you have or have you had an identical twin brother or sister?

integer

genetic_17 (VAR_NAMES)
Do you have or have you had an identical twin brother or sister? (LABEL)
integer (DATA_TYPE)
1=yes|0=no|999=not stated (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1970 (VARIABLE_ORDER)
Haben oder hatten Sie einen eineiigen Zwillingsbruder oder eine eineiige Zwillingsschwester? (LABEL_DE)
1=ja|0=nein|999=keine Angabe (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_17 (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.123

Code List

Do you have or have you had an identical twin brother or sister?

CL Item

yes (1)

CL Item

no (0)

CL Item

not stated (999)

genetic_18

Item

Do any diseases typically referred to as hereditary diseases occur in your further relatives - by this I mean blood relatives such as grandparents, uncles, aunts?

integer

genetic_18 (VAR_NAMES)
Do any diseases typically referred to as hereditary diseases occur in your further relatives - by this I mean blood relatives such as grandparents, uncles, aunts? (LABEL)
integer (DATA_TYPE)
1=yes|0=no|999=not stated (VALUE_LABELS)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1980 (VARIABLE_ORDER)
Kommen in Ihrer weiteren Verwandtschaft - damit meine ich Blutsverwandte wie Großeltern, Onkel, Tanten - irgendwelche Erkrankungen vor, die typischerweise als Erbkrankheit bezeichnet werden? (LABEL_DE)
1=ja|0=nein|999=keine Angabe (VALUE_LABELS_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_18 (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

CL.123

Code List

Do any diseases typically referred to as hereditary diseases occur in your further relatives - by this I mean blood relatives such as grandparents, uncles, aunts?

CL Item

yes (1)

CL Item

no (0)

CL Item

not stated (999)

genetic_18a

Item

What diseases are we talking about?

string

genetic_18a (VAR_NAMES)
What diseases are we talking about? (LABEL)
string (DATA_TYPE)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
1990 (VARIABLE_ORDER)
Um welche Erkrankungen handelt es sich da? (LABEL_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_18a (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

genetic_18b

Item

Who suffers or suffered from them?

string

genetic_18b (VAR_NAMES)
Who suffers or suffered from them? (LABEL)
string (DATA_TYPE)
missing_table_3039 (MISSING_LIST_TABLE)
x0.end_dat (TIME_VAR)
x0.body_genetic (STUDY_SEGMENT)
2000 (VARIABLE_ORDER)
Wer leidet oder litt darunter? (LABEL_DE)
SAQ_NEXT (REPORT_NAME)
T_SAQ_NEXT (TABLE_NAME)
x0.genetic_18b (UNIQUE_NAME)
NEXT (SOURCE)
NEXT-0 (DCE)
NEXT|NEXT0|SAQ|SAQ_NEXT|BODY_GENETIC (HIERARCHY)

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