Item Group
Inclusion and exclusion criteria
C1512693 (UMLS CUI [1,1])
C0680251 (UMLS CUI [1,2])
Inclusion criteria: All individuals have the 3 million base pair 22q11.2 deletion on one allele of chromosome 22. They are all unrelated subjects that have enrolled in the research study with their informed consent and are de-identified for research. They have known cardiac phenotype clinical information. Either gender was included. The subjects are self-reported as Caucasian.
Item
Inclusion criteria: All individuals have the 3 million base pair 22q11.2 deletion on one allele of chromosome 22. They are all unrelated subjects that have enrolled in the research study with their informed consent and are de-identified for research. They have known cardiac phenotype clinical information. Either gender was included. The subjects are self-reported as Caucasian.
boolean
C1512693 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
C4759731 (UMLS CUI [1,3])
C4521766 (UMLS CUI [1,4])
C0008665 (UMLS CUI [1,5])
C0002085 (UMLS CUI [1,6])
C0445356 (UMLS CUI [2,1])
C4684790 (UMLS CUI [2,2])
C0021430 (UMLS CUI [2,3])
C4684638 (UMLS CUI [2,4])
C0035168 (UMLS CUI [2,5])
C0031437 (UMLS CUI [3,1])
C1522601 (UMLS CUI [3,2])
C2708733 (UMLS CUI [3,3])
C1512693 (UMLS CUI [4,1])
C0079399 (UMLS CUI [4,2])
C5707708 (UMLS CUI [4,3])
C4540954 (UMLS CUI [4,4])
Exclusion criteria would be an individual that does not have a 22q11.2 deletion or has unknown cardiac phenotype information.
Item
Exclusion criteria would be an individual that does not have a 22q11.2 deletion or has unknown cardiac phenotype information.
boolean
C0680251 (UMLS CUI [1,1])
C1518422 (UMLS CUI [1,2])
C4521766 (UMLS CUI [1,3])
C0439673 (UMLS CUI [1,4])
C0031437 (UMLS CUI [1,5])
C1522601 (UMLS CUI [1,6])