Item
Zuckerkrankheit (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)
Code List
Zuckerkrankheit (Diabetes mellitus)
CL Item
keine Angabe (999)
Item
Zuckerkrankheit (Diabetes mellitus) [Vater]
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)
Code List
Zuckerkrankheit (Diabetes mellitus) [Vater]
Item
Zuckerkrankheit (Diabetes mellitus) [Mutter]
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)
Code List
Zuckerkrankheit (Diabetes mellitus) [Mutter]
Item
Zuckerkrankheit (Diabetes mellitus) [Geschwister]
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)
Code List
Zuckerkrankheit (Diabetes mellitus) [Geschwister]
Item
Zuckerkrankheit (Diabetes mellitus) [Kinder]
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)
Code List
Zuckerkrankheit (Diabetes mellitus) [Kinder]
Item
Zuckerkrankheit (Diabetes mellitus) [keine Angabe]
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)
Code List
Zuckerkrankheit (Diabetes mellitus) [keine Angabe]
Item
Hoher Blutdruck
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)
Code List
Hoher Blutdruck
CL Item
keine Angabe (999)
Item
Hoher Blutdruck [Vater]
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)
Code List
Hoher Blutdruck [Vater]
Item
Hoher Blutdruck [Mutter]
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)
Code List
Hoher Blutdruck [Mutter]
Item
Hoher Blutdruck [Geschwister]
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)
Code List
Hoher Blutdruck [Geschwister]
Item
Hoher Blutdruck [Kinder]
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)
Code List
Hoher Blutdruck [Kinder]
Item
Hoher Blutdruck [keine Angabe]
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)
Code List
Hoher Blutdruck [keine Angabe]
Item
Herzinfarkt
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 Item
keine Angabe (999)
Item
Herzinfarkt [Vater]
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)
Code List
Herzinfarkt [Vater]
Item
Herzinfarkt [Mutter]
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)
Code List
Herzinfarkt [Mutter]
Item
Herzinfarkt [Geschwister]
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)
Code List
Herzinfarkt [Geschwister]
Item
Herzinfarkt [Kinder]
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)
Code List
Herzinfarkt [Kinder]
Item
Herzinfarkt [keine Angabe]
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)
Code List
Herzinfarkt [keine Angabe]
Item
Schlaganfall
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 Item
keine Angabe (999)
Item
Schlaganfall [Vater]
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)
Code List
Schlaganfall [Vater]
Item
Schlaganfall [Mutter]
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)
Code List
Schlaganfall [Mutter]
Item
Schlaganfall [Geschwister]
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)
Code List
Schlaganfall [Geschwister]
Item
Schlaganfall [Kinder]
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)
Code List
Schlaganfall [Kinder]
Item
Schlaganfall [keine Angabe]
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)
Code List
Schlaganfall [keine Angabe]
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 Item
keine Angabe (999)
Item
Asthma [Vater]
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)
Item
Asthma [Mutter]
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)
Code List
Asthma [Mutter]
Item
Asthma [Geschwister]
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)
Code List
Asthma [Geschwister]
Item
Asthma [Kinder]
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)
Code List
Asthma [Kinder]
Item
Asthma [keine Angabe]
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)
Code List
Asthma [keine Angabe]
Item
Blutgerinnungsstörungen, z. B. Bluter
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)
Code List
Blutgerinnungsstörungen, z. B. Bluter
CL Item
keine Angabe (999)
Item
Blutgerinnungsstörungen, z. B. Bluter [Vater]
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)
Code List
Blutgerinnungsstörungen, z. B. Bluter [Vater]
Item
Blutgerinnungsstörungen, z. B. Bluter [Mutter]
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)
Code List
Blutgerinnungsstörungen, z. B. Bluter [Mutter]
Item
Blutgerinnungsstörungen, z. B. Bluter [Geschwister]
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)
Code List
Blutgerinnungsstörungen, z. B. Bluter [Geschwister]
Item
Blutgerinnungsstörungen, z. B. Bluter [Kinder]
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)
Code List
Blutgerinnungsstörungen, z. B. Bluter [Kinder]
Item
Blutgerinnungsstörungen, z. B. Bluter [keine Angabe]
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)
Code List
Blutgerinnungsstörungen, z. B. Bluter [keine Angabe]
Item
Muskelerkrankungen, z. B. Muskelschwäche
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)
Code List
Muskelerkrankungen, z. B. Muskelschwäche
CL Item
keine Angabe (999)
Item
Muskelerkrankungen, z. B. Muskelschwäche [Vater]
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)
Code List
Muskelerkrankungen, z. B. Muskelschwäche [Vater]
Item
Muskelerkrankungen, z. B. Muskelschwäche [Mutter]
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)
Code List
Muskelerkrankungen, z. B. Muskelschwäche [Mutter]
Item
Muskelerkrankungen, z. B. Muskelschwäche [Geschwister]
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)
Code List
Muskelerkrankungen, z. B. Muskelschwäche [Geschwister]
Item
Muskelerkrankungen, z. B. Muskelschwäche [Kinder]
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)
Code List
Muskelerkrankungen, z. B. Muskelschwäche [Kinder]
Item
Muskelerkrankungen, z. B. Muskelschwäche [keine Angabe]
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)
Code List
Muskelerkrankungen, z. B. Muskelschwäche [keine Angabe]
Item
Parkinson’sche Erkrankung (Schüttellähmung)
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)
Code List
Parkinson’sche Erkrankung (Schüttellähmung)
CL Item
keine Angabe (999)
Item
Parkinson’sche Erkrankung (Schüttellähmung) [Vater]
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)
Code List
Parkinson’sche Erkrankung (Schüttellähmung) [Vater]
Item
Parkinson’sche Erkrankung (Schüttellähmung) [Mutter]
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)
Code List
Parkinson’sche Erkrankung (Schüttellähmung) [Mutter]
Item
Parkinson’sche Erkrankung (Schüttellähmung) [Geschwister]
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)
Code List
Parkinson’sche Erkrankung (Schüttellähmung) [Geschwister]
Item
Parkinson’sche Erkrankung (Schüttellähmung) [Kinder]
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)
Code List
Parkinson’sche Erkrankung (Schüttellähmung) [Kinder]
Item
Parkinson’sche Erkrankung (Schüttellähmung) [keine Angabe]
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)
Code List
Parkinson’sche Erkrankung (Schüttellähmung) [keine Angabe]
Item
Geistesschwäche, z. B. Alzheimer
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)
Code List
Geistesschwäche, z. B. Alzheimer
CL Item
keine Angabe (999)
Item
Geistesschwäche, z. B. Alzheimer [Vater]
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)
Code List
Geistesschwäche, z. B. Alzheimer [Vater]
Item
Geistesschwäche, z. B. Alzheimer [Mutter]
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)
Code List
Geistesschwäche, z. B. Alzheimer [Mutter]
Item
Geistesschwäche, z. B. Alzheimer [Geschwister]
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)
Code List
Geistesschwäche, z. B. Alzheimer [Geschwister]
Item
Geistesschwäche, z. B. Alzheimer [Kinder]
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)
Code List
Geistesschwäche, z. B. Alzheimer [Kinder]
Item
Geistesschwäche, z. B. Alzheimer [keine Angabe]
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)
Code List
Geistesschwäche, z. B. Alzheimer [keine Angabe]
Item
Epilepsie, d. h. Anfallsleiden
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)
Code List
Epilepsie, d. h. Anfallsleiden
CL Item
keine Angabe (999)
Item
Epilepsie, d. h. Anfallsleiden [Vater]
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)
Code List
Epilepsie, d. h. Anfallsleiden [Vater]
Item
Epilepsie, d. h. Anfallsleiden [Mutter]
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)
Code List
Epilepsie, d. h. Anfallsleiden [Mutter]
Item
Epilepsie, d. h. Anfallsleiden [Geschwister]
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)
Code List
Epilepsie, d. h. Anfallsleiden [Geschwister]
Item
Epilepsie, d. h. Anfallsleiden [Kinder]
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)
Code List
Epilepsie, d. h. Anfallsleiden [Kinder]
Item
Epilepsie, d. h. Anfallsleiden [keine Angabe]
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)
Code List
Epilepsie, d. h. Anfallsleiden [keine Angabe]
Item
Krebserkrankung
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)
Code List
Krebserkrankung
CL Item
keine Angabe (999)
Item
Krebserkrankung [Vater]
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)
Code List
Krebserkrankung [Vater]
Item
Krebserkrankung [Mutter]
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)
Code List
Krebserkrankung [Mutter]
Item
Krebserkrankung [Geschwister]
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)
Code List
Krebserkrankung [Geschwister]
Item
Krebserkrankung [Kinder]
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)
Code List
Krebserkrankung [Kinder]
Item
Krebserkrankung [keine Angabe]
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)
Code List
Krebserkrankung [keine Angabe]
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
Welche Krebserkrankung hat Ihre Mutter?
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
Welche Krebserkrankung haben Ihre Geschwister?
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
Welche Krebserkrankung haben Ihre Kinder?
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)
Item
Angeborene körperliche Fehlbildungen
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)
Code List
Angeborene körperliche Fehlbildungen
CL Item
keine Angabe (999)
Item
Angeborene körperliche Fehlbildungen [Vater]
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)
Code List
Angeborene körperliche Fehlbildungen [Vater]
Item
Angeborene körperliche Fehlbildungen [Mutter]
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)
Code List
Angeborene körperliche Fehlbildungen [Mutter]
Item
Angeborene körperliche Fehlbildungen [Geschwister]
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)
Code List
Angeborene körperliche Fehlbildungen [Geschwister]
Item
Angeborene körperliche Fehlbildungen [Kinder]
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)
Code List
Angeborene körperliche Fehlbildungen [Kinder]
Item
Angeborene körperliche Fehlbildungen [keine Angabe]
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)
Code List
Angeborene körperliche Fehlbildungen [keine Angabe]
genetic_12a1
Item
Welche angeborene körperliche Fehlbildung hat Ihr Vater?
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
Welche angeborene körperliche Fehlbildung hat Ihre Mutter?
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
Welche angeborenen körperlichen Fehlbildungen haben Ihre Geschwister?
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
Welche angeborenen körperlichen Fehlbildungen haben Ihre Kinder?
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)
Item
Allergien
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 Item
keine Angabe (999)
Item
Allergien [Vater]
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)
Code List
Allergien [Vater]
Item
Allergien [Mutter]
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)
Code List
Allergien [Mutter]
Item
Allergien [Geschwister]
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)
Code List
Allergien [Geschwister]
Item
Allergien [Kinder]
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)
Code List
Allergien [Kinder]
Item
Allergien [keine Angabe]
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)
Code List
Allergien [keine Angabe]
genetic_13a1
Item
Welche Allergien hat Ihr Vater?
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
Welche Allergien hat Ihre Mutter?
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
Welche Allergien haben Ihre Geschwister?
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
Welche Allergien haben Ihre Kinder?
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)
Item
Gallensteinleiden
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)
Code List
Gallensteinleiden
CL Item
keine Angabe (999)
Item
Gallensteinleiden [Vater]
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)
Code List
Gallensteinleiden [Vater]
Item
Gallensteinleiden [Mutter]
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)
Code List
Gallensteinleiden [Mutter]
Item
Gallensteinleiden [Geschwister]
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)
Code List
Gallensteinleiden [Geschwister]
Item
Gallensteinleiden [Kinder]
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)
Code List
Gallensteinleiden [Kinder]
Item
Gallensteinleiden [keine Angabe]
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)
Code List
Gallensteinleiden [keine Angabe]
Item
Gicht
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 Item
keine Angabe (999)
Item
Gicht [Vater]
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)
Item
Gicht [Mutter]
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)
Item
Gicht [Geschwister]
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)
Code List
Gicht [Geschwister]
Item
Gicht [Kinder]
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)
Item
Gicht [keine Angabe]
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)
Code List
Gicht [keine Angabe]
genetic_16
Item
Wie viele leibliche Geschwister (keine Halbgeschwister) haben oder hatten Sie?
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)
Item
Haben oder hatten Sie einen eineiigen Zwillingsbruder oder eine eineiige Zwillingsschwester?
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)
Code List
Haben oder hatten Sie einen eineiigen Zwillingsbruder oder eine eineiige Zwillingsschwester?
CL Item
keine Angabe (999)
Item
Kommen in Ihrer weiteren Verwandtschaft - damit meine ich Blutsverwandte wie Großeltern, Onkel, Tanten - irgendwelche Erkrankungen vor, die typischerweise als Erbkrankheit bezeichnet werden?
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)
Code List
Kommen in Ihrer weiteren Verwandtschaft - damit meine ich Blutsverwandte wie Großeltern, Onkel, Tanten - irgendwelche Erkrankungen vor, die typischerweise als Erbkrankheit bezeichnet werden?
CL Item
keine Angabe (999)
genetic_18a
Item
Um welche Erkrankungen handelt es sich da?
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
Wer leidet oder litt darunter?
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)