Subject ID, race, country of residence, whether genotyping is performed, sex, child primary diagnosis, height, weight, tanner stage, and laboratory tests of participants with or without chronic kidney disease and involved in the "Pediatric Investigation for Genetic Factors Linked with Renal Disease Progression (PediGFR), version with Cardiovascular Comorbidity in Children with Chronic Kidney Disease (4C) Study" project.

  1. StudyEvent: SEV1
    1. Eligibility Criteria
    2. Subject ID, race, gender, whether genotyping is performed, child primary diagnosis, height, weight, tanner stage, and laboratory tests of participants with or without chronic kidney disease and involved in the "Pediatric Investigation for Genetic Factors Linked with Renal Progression (PediGFR), version with Chronic Kidney Disease in Children Cohort (CKiD)" project.
    3. Sample ID, analyte type, body site where sample was obtained, histological type of sample, and tumor status of sample of participants with or without chronic kidney disease and involved in the "Pediatric Investigation for Genetic Factors Linked with Renal Progression (PediGFR), version with Chronic Kidney Disease in Children Cohort (CKiD)" project.
    4. Subject ID, subject source, source subject ID, and consent group of participants with or without chronic kidney disease and involved in the "Pediatric Investigation for Genetic Factors Linked with Renal Progression (PediGFR)" project.
    5. Subject ID, sample ID, sample use, and study accession ID of participants with or without chronic kidney disease and involved in the "Pediatric Investigation for Genetic Factors Linked with Renal Progression (PediGFR)" project.
    6. Subject ID, race, country of residence, whether genotyping is performed, sex, child primary diagnosis, height, weight, tanner stage, and laboratory tests of participants with or without chronic kidney disease and involved in the "Pediatric Investigation for Genetic Factors Linked with Renal Disease Progression (PediGFR), version with Cardiovascular Comorbidity in Children with Chronic Kidney Disease (4C) Study" project.
    7. Sample ID, analyte type, body site where sample was obtained, histological type of sample, and tumor status of sample of participants with or without chronic kidney disease and involved in the "Pediatric Investigation for Genetic Factors Linked with Renal Disease Progression (PediGFR), version with Cardiovascular Comorbidity in Children with Chronic Kidney Disease (4C) Study" project.
    8. Subject ID, country of residence, whether genotyping is performed, gender, child primary diagnosis, height, weight, tanner stage, and laboratory tests of participants with or without chronic kidney disease and involved in the "Pediatric Investigation for Genetic Factors Linked with Renal Disease Progression (PediGFR), version with Effect of Strict Blood Pressure Control and ACE Inhibition on the Progression of CRF in Pediatric Patients (ESCAPE) Trial" project.
    9. Sample ID, analyte type, body site where sample was obtained, histological type of sample, and tumor status of samples obtained from participants with or without chronic kidney disease and involved in the "Pediatric Investigation for Genetic Factors Linked with Renal Disease Progression (PediGFR), version with Effect of Strict Blood Pressure Control and ACE Inhibition on the Progression of CRF in Pediatric Patients (ESCAPE) Trial" project.
pht004404
Descrizione

pht004404

Alias
UMLS CUI [1,1]
C3846158
Child sex
Descrizione

MALE1FE2

Tipo di dati

text

Alias
UMLS CUI [1,1]
C0079399
Child Primary Diagnosis (Grouped categories)
Descrizione

rendiag

Tipo di dati

text

Alias
UMLS CUI [1,1]
C0332137
Primary CKD diagnosis code
Descrizione

primdx

Tipo di dati

text

Alias
UMLS CUI [1,1]
C0277554
UMLS CUI [1,2]
C1561643
UMLS CUI [1,3]
C1550350
Child Primary Diagnosis (Grouped categories, diseases affecting the glomerulus vs. no)
Descrizione

gngdiag

Tipo di dati

text

Alias
UMLS CUI [1,1]
C0332137
Height
Descrizione

height

Tipo di dati

float

Unità di misura
  • cm
Alias
UMLS CUI [1,1]
C0005890
cm
Weight
Descrizione

weight

Tipo di dati

float

Unità di misura
  • kg
Alias
UMLS CUI [1,1]
C0005910
kg
Tanner Stage
Descrizione

tanner

Tipo di dati

text

Alias
UMLS CUI [1,1]
C2826146
Estimated GFR
Descrizione

egfr

Tipo di dati

float

Unità di misura
  • ml/min/1.73m2
Alias
UMLS CUI [1,1]
C3811844
ml/min/1.73m2
Serum Creatinine, collected
Descrizione

scr

Tipo di dati

float

Unità di misura
  • mg/dl
Alias
UMLS CUI [1,1]
C0201976
mg/dl
Cystatin C
Descrizione

CyC

Tipo di dati

float

Alias
UMLS CUI [1,1]
C1619716
Urea
Descrizione

urea

Tipo di dati

float

Unità di misura
  • mg/dl
Alias
UMLS CUI [1,1]
C0523961
mg/dl
BUN
Descrizione

BUN

Tipo di dati

float

Alias
UMLS CUI [1,1]
C0005845
Urine Albumin/Creatinine
Descrizione

ualbcr

Tipo di dati

float

Alias
UMLS CUI [1,1]
C1096054
Child's race
Descrizione

race

Tipo di dati

text

Alias
UMLS CUI [1,1]
C0034510
Child of Hispanic/Latino
Descrizione

Hisp

Tipo di dati

text

Alias
UMLS CUI [1,1]
C0008059
UMLS CUI [1,2]
C0086409
UMLS CUI [1,3]
C0086528
Whether genotyping is performed on the subject?
Descrizione

genotyped

Tipo di dati

text

Alias
UMLS CUI [1,1]
C1285573
UMLS CUI [1,2]
C0884358
Country of residence (given by responsible study center)
Descrizione

country

Tipo di dati

text

Alias
UMLS CUI [1,1]
C3258975
De-identified subject ID
Descrizione

SUBJECT_ID

Tipo di dati

string

Alias
UMLS CUI [1,1]
C4684638
UMLS CUI [1,2]
C2348585

Similar models

Subject ID, race, country of residence, whether genotyping is performed, sex, child primary diagnosis, height, weight, tanner stage, and laboratory tests of participants with or without chronic kidney disease and involved in the "Pediatric Investigation for Genetic Factors Linked with Renal Disease Progression (PediGFR), version with Cardiovascular Comorbidity in Children with Chronic Kidney Disease (4C) Study" project.

  1. StudyEvent: SEV1
    1. Eligibility Criteria
    2. Subject ID, race, gender, whether genotyping is performed, child primary diagnosis, height, weight, tanner stage, and laboratory tests of participants with or without chronic kidney disease and involved in the "Pediatric Investigation for Genetic Factors Linked with Renal Progression (PediGFR), version with Chronic Kidney Disease in Children Cohort (CKiD)" project.
    3. Sample ID, analyte type, body site where sample was obtained, histological type of sample, and tumor status of sample of participants with or without chronic kidney disease and involved in the "Pediatric Investigation for Genetic Factors Linked with Renal Progression (PediGFR), version with Chronic Kidney Disease in Children Cohort (CKiD)" project.
    4. Subject ID, subject source, source subject ID, and consent group of participants with or without chronic kidney disease and involved in the "Pediatric Investigation for Genetic Factors Linked with Renal Progression (PediGFR)" project.
    5. Subject ID, sample ID, sample use, and study accession ID of participants with or without chronic kidney disease and involved in the "Pediatric Investigation for Genetic Factors Linked with Renal Progression (PediGFR)" project.
    6. Subject ID, race, country of residence, whether genotyping is performed, sex, child primary diagnosis, height, weight, tanner stage, and laboratory tests of participants with or without chronic kidney disease and involved in the "Pediatric Investigation for Genetic Factors Linked with Renal Disease Progression (PediGFR), version with Cardiovascular Comorbidity in Children with Chronic Kidney Disease (4C) Study" project.
    7. Sample ID, analyte type, body site where sample was obtained, histological type of sample, and tumor status of sample of participants with or without chronic kidney disease and involved in the "Pediatric Investigation for Genetic Factors Linked with Renal Disease Progression (PediGFR), version with Cardiovascular Comorbidity in Children with Chronic Kidney Disease (4C) Study" project.
    8. Subject ID, country of residence, whether genotyping is performed, gender, child primary diagnosis, height, weight, tanner stage, and laboratory tests of participants with or without chronic kidney disease and involved in the "Pediatric Investigation for Genetic Factors Linked with Renal Disease Progression (PediGFR), version with Effect of Strict Blood Pressure Control and ACE Inhibition on the Progression of CRF in Pediatric Patients (ESCAPE) Trial" project.
    9. Sample ID, analyte type, body site where sample was obtained, histological type of sample, and tumor status of samples obtained from participants with or without chronic kidney disease and involved in the "Pediatric Investigation for Genetic Factors Linked with Renal Disease Progression (PediGFR), version with Effect of Strict Blood Pressure Control and ACE Inhibition on the Progression of CRF in Pediatric Patients (ESCAPE) Trial" project.
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
pht004404
C3846158 (UMLS CUI [1,1])
Item
Child sex
text
C0079399 (UMLS CUI [1,1])
Code List
Child sex
CL Item
Male (1)
C0086582 (UMLS CUI [1,1])
CL Item
Female (2)
C0086287 (UMLS CUI [1,1])
Item
Child Primary Diagnosis (Grouped categories)
text
C0332137 (UMLS CUI [1,1])
Code List
Child Primary Diagnosis (Grouped categories)
CL Item
CAKUT (1)
CL Item
Glomerulopathies (2)
CL Item
Hemolytic uremic syndrome (3)
CL Item
Nephronophthisis (4)
C3846158 (UMLS CUI [1,1])
CL Item
oxalosis or cystinosis (metabolic disease) (5)
CL Item
Polycystic kidney disease (6)
CL Item
Alport disease (7)
CL Item
Vasculitis (8)
CL Item
other (9)
Item
Primary CKD diagnosis code
text
C0277554 (UMLS CUI [1,1])
C1561643 (UMLS CUI [1,2])
C1550350 (UMLS CUI [1,3])
Code List
Primary CKD diagnosis code
CL Item
Focal segmental glomerulosclerosis (10)
CL Item
Hemolytic uremic syndrome (11)
CL Item
Familial nephritis (Alport's) (12)
CL Item
IgA Nephropathy (Berger's) (13)
CL Item
Systemic immunological disease (including SLE) (14)
CL Item
Chronic glomerulonephritis (15)
CL Item
Membranoproliferative glomerulonephritis type I (16)
CL Item
Idiopathic crescentic glomerulonephritis (17)
CL Item
Membranous nephropathy (18)
CL Item
Henoch schonlein nephritis (19)
CL Item
Congenital nephrotic syndrome (20)
CL Item
Membranoproliferative glomerulonephritis type II (21)
CL Item
Sickle cell nephropathy (22)
CL Item
Denys-Drash syndrome (23)
CL Item
Diabetic nephropathy (24)
CL Item
Glomerular Other (40)
CL Item
Obstructive uropathy (50)
CL Item
Aplastic/hypoplastic/ dysplastic kidneys (51)
CL Item
Reflux nephropathy (52)
CL Item
Polycystic kidney disease (Autosomal recessive) (53)
CL Item
Cystinosis (54)
CL Item
Pyelonephritis/ Interstitial nephritis (55)
CL Item
Renal infarct (56)
CL Item
Medullary cystic disease/ Juvenile nephronophthisis (57)
C3846158 (UMLS CUI [1,1])
CL Item
Syndrome of agenesis of abdominal musculature (58)
CL Item
Wilms' tumor (59)
CL Item
Polycystic kidney disease (Autosomal dominant) (60)
CL Item
Oxalosis (61)
CL Item
Non-Glomerular Other (80)
CL Item
No match for original diagnosis available by CKiD coding system (99)
Item
Child Primary Diagnosis (Grouped categories, diseases affecting the glomerulus vs. no)
text
C0332137 (UMLS CUI [1,1])
Code List
Child Primary Diagnosis (Grouped categories, diseases affecting the glomerulus vs. no)
CL Item
Glom (HUS) (1)
CL Item
Glom (NOT HUS) (2)
CL Item
Non-glom (GU, Cystic, Hereditary) (3)
CL Item
Non-glom (NOT GU, NOT Cystic, NOT Hereditary) (4)
height
Item
Height
float
C0005890 (UMLS CUI [1,1])
weight
Item
Weight
float
C0005910 (UMLS CUI [1,1])
Item
Tanner Stage
text
C2826146 (UMLS CUI [1,1])
Code List
Tanner Stage
CL Item
Missing (-9)
CL Item
Stage 1 (1)
CL Item
Stage 2 (2)
CL Item
Stage 3 (3)
CL Item
Stage 4 (4)
CL Item
Stage 5 (5)
egfr
Item
Estimated GFR
float
C3811844 (UMLS CUI [1,1])
scr
Item
Serum Creatinine, collected
float
C0201976 (UMLS CUI [1,1])
CyC
Item
Cystatin C
float
C1619716 (UMLS CUI [1,1])
urea
Item
Urea
float
C0523961 (UMLS CUI [1,1])
BUN
Item
BUN
float
C0005845 (UMLS CUI [1,1])
ualbcr
Item
Urine Albumin/Creatinine
float
C1096054 (UMLS CUI [1,1])
Item
Child's race
text
C0034510 (UMLS CUI [1,1])
Code List
Child's race
CL Item
Missing (-9)
CL Item
Caucasian (1)
CL Item
East Asian (2)
CL Item
Hispanic (3)
CL Item
Indian (4)
CL Item
Arabic (5)
CL Item
African /African American (6)
CL Item
Other (7)
Item
Child of Hispanic/Latino
text
C0008059 (UMLS CUI [1,1])
C0086409 (UMLS CUI [1,2])
C0086528 (UMLS CUI [1,3])
Code List
Child of Hispanic/Latino
CL Item
No (0)
CL Item
Yes (1)
Item
Whether genotyping is performed on the subject?
text
C1285573 (UMLS CUI [1,1])
C0884358 (UMLS CUI [1,2])
Code List
Whether genotyping is performed on the subject?
CL Item
No (0)
CL Item
Yes (1)
Item
Country of residence (given by responsible study center)
text
C3258975 (UMLS CUI [1,1])
Code List
Country of residence (given by responsible study center)
CL Item
Austria (AT)
CL Item
Switzerland (CH)
CL Item
Czech Republic (CZ)
CL Item
Germany (DE)
CL Item
France (FR)
CL Item
Hungary (HU)
CL Item
Italy (IT)
CL Item
Lithuania (LT)
CL Item
Poland (PL)
CL Item
Portugal (PT)
CL Item
Serbia (RS)
CL Item
Turkey (TR)
CL Item
United Kingdom (UK)
SUBJECT_ID
Item
De-identified subject ID
string
C4684638 (UMLS CUI [1,1])
C2348585 (UMLS CUI [1,2])