ID

45934

Description

Principal Investigator: Bernice Morrow, PhD, Albert Einstein College of Medicine, Bronx, NY, USA MeSH: Tetralogy of Fallot,Psychotic Disorders,Schizophrenia,Arthritis, Juvenile https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000837 Two subjects with 22q11.2 deletion syndromes (22q11DS) and their parents were recruited for a whole genome sequencing study to identify candidate genetic modifiers of the various phenotypes seen in 22q11DS. Both probands had a typical 3 megabase deletion on chromosome 22q11.2 but discordant phenotypes.

Link

dbGaP study=phs000837

Keywords

  1. 3/9/24 3/9/24 - Madita Rudolph
Copyright Holder

Bernice Morrow, PhD, Albert Einstein College of Medicine, Bronx, NY, USA

Uploaded on

March 9, 2024

DOI

To request one please log in.

License

Creative Commons BY 4.0

Model comments :

You can comment on the data model here. Via the speech bubbles at the itemgroups and items you can add comments to those specificially.

Itemgroup comments for :

Item comments for :

In order to download data models you must be logged in. Please log in or register for free.

dbGaP phs000837 Whole Genome Sequencing of Two 22q11DS Trios

Eligibility Criteria

Inclusion and exclusion criteria
Description

Inclusion and exclusion criteria

Alias
UMLS CUI [1,1]
C1512693
UMLS CUI [1,2]
C0680251
Inclusion criteria: Probands diagnosed with 22q11.2 deletion syndrome and has 3 megabase deletion on chromosome 22q11.2 confirmed by fluorescence *in situ* hybridization. Both parents are available for DNA collection and are unaffected.
Description

Elig.phs000837.v1.p1.1

Data type

boolean

Alias
UMLS CUI [1,1]
C1512693
UMLS CUI [1,2]
C1997894
UMLS CUI [1,3]
C4521766
UMLS CUI [1,4]
C0752096
UMLS CUI [1,5]
C0162789
UMLS CUI [2,1]
C1512693
UMLS CUI [2,2]
C0470187
UMLS CUI [2,3]
C1706086
UMLS CUI [2,4]
C0030551
UMLS CUI [2,5]
C1561491
UMLS CUI [2,6]
C2986417
Exclusion criteria: Probands with alternate or atypical 22q11.2 deletions. Parents unavailable for sequencing.
Description

Elig.phs000837.v1.p1.2

Data type

boolean

Alias
UMLS CUI [1,1]
C0680251
UMLS CUI [1,2]
C1997894
UMLS CUI [1,3]
C0205182
UMLS CUI [1,4]
C4521766
UMLS CUI [2,1]
C0680251
UMLS CUI [2,2]
C0686905
UMLS CUI [2,3]
C0030551
UMLS CUI [2,4]
C1561491

Similar models

Eligibility Criteria

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Inclusion and exclusion criteria
C1512693 (UMLS CUI [1,1])
C0680251 (UMLS CUI [1,2])
Elig.phs000837.v1.p1.1
Item
Inclusion criteria: Probands diagnosed with 22q11.2 deletion syndrome and has 3 megabase deletion on chromosome 22q11.2 confirmed by fluorescence *in situ* hybridization. Both parents are available for DNA collection and are unaffected.
boolean
C1512693 (UMLS CUI [1,1])
C1997894 (UMLS CUI [1,2])
C4521766 (UMLS CUI [1,3])
C0752096 (UMLS CUI [1,4])
C0162789 (UMLS CUI [1,5])
C1512693 (UMLS CUI [2,1])
C0470187 (UMLS CUI [2,2])
C1706086 (UMLS CUI [2,3])
C0030551 (UMLS CUI [2,4])
C1561491 (UMLS CUI [2,5])
C2986417 (UMLS CUI [2,6])
Elig.phs000837.v1.p1.2
Item
Exclusion criteria: Probands with alternate or atypical 22q11.2 deletions. Parents unavailable for sequencing.
boolean
C0680251 (UMLS CUI [1,1])
C1997894 (UMLS CUI [1,2])
C0205182 (UMLS CUI [1,3])
C4521766 (UMLS CUI [1,4])
C0680251 (UMLS CUI [2,1])
C0686905 (UMLS CUI [2,2])
C0030551 (UMLS CUI [2,3])
C1561491 (UMLS CUI [2,4])

Please use this form for feedback, questions and suggestions for improvements.

Fields marked with * are required.

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial