Elig.phs001089.v4.p1.2
Item
Parent(s) or guardian(s) is ≥ 19 years of age. If parent is a biological parent and wishes to participate in the study, parent is competent to consent to her/his own research participation.
boolean
C0021430 (UMLS CUI [1,1])
C0030551 (UMLS CUI [1,2])
C1274041 (UMLS CUI [1,3])
Elig.phs001089.v4.p1.3
Item
If parent is a biological parent and wishes to participate in the study, parent is willing to have blood drawn and receive genetic results.
boolean
C0005834 (UMLS CUI [1,1])
C0679560 (UMLS CUI [1,2])
Elig.phs001089.v4.p1.4
Item
Parent(s) or guardian(s) is willing to complete two clinic visits (one for consent and blood draw, another for return of genetic results).
boolean
C0525058 (UMLS CUI [1,1])
Elig.phs001089.v4.p1.5
Item
Parent(s) or guardian(s) with custodial authority are willing to consent to the proband child's participation.
boolean
C0021430 (UMLS CUI [1,1])
C0030551 (UMLS CUI [1,2])
C1274041 (UMLS CUI [1,3])
Elig.phs001089.v4.p1.6
Item
Parent(s) or guardian(s) is able to communicate in English.
boolean
C2364293 (UMLS CUI [1,1])
C0376245 (UMLS CUI [1,2])
Elig.phs001089.v4.p1.7
Item
Child weighs ≥ 9 kilos (19.8 lbs.)
boolean
C0005910 (UMLS CUI [1,1])
Elig.phs001089.v4.p1.8
Item
Has at least one parent or guardian able to consent to his or her participation in study.
boolean
C0021430 (UMLS CUI [1,1])
C0030551 (UMLS CUI [1,2])
C1274041 (UMLS CUI [1,3])
Elig.phs001089.v4.p1.9
Item
Child has been diagnosed with a significant developmental delay and/or intellectual disability, with or without congenital structural or functional anomalies.
boolean
C0424605 (UMLS CUI [1,1])
C3714756 (UMLS CUI [1,2])
Elig.phs001089.v4.p1.10
Item
Proband child's parent(s) or guardian(s) unable or unwilling to consent to child's participation.
boolean
C0021430 (UMLS CUI [1,1])
C0558080 (UMLS CUI [1,2])
C0030551 (UMLS CUI [1,3])
C1274041 (UMLS CUI [1,4])
Elig.phs001089.v4.p1.11
Item
A specific genetic or environmental etiology for DD/ID or rare undiagnosed disease has already been diagnosed (including genetic or chromosomal syndromes or teratogen exposure syndromes).
boolean
C0205309 (UMLS CUI [1,1])
C0011900 (UMLS CUI [1,2])
C0008626 (UMLS CUI [1,3])
C0743662 (UMLS CUI [1,4])