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UMLS. CSP-HL7-ICD9CM-NCI-NDFRT-RXNORM
%
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
V V- V0 V1 V2 VA VC VD VE VF VH VI VJ VK VM VN VO VP VQ VR VS VT VU VV VX VY
VE VEA VEC VED VEE VEG VEH VEI VEL VEN VEP VER VES VET

VELO-CARDIO-FACIAL SYND

[caused by microdeletion on chromosome 22q11.2; associated with multiple congenital anomalies, learning disabilities, behavioral phenotypes including ADHD and anxiety, with schizophrenic risk in adulthood. ( CSP )]
UMLS (ICD9CM) C0220704
 
Congenital Abnormality
Disease or Syndrome
Relation/PAR: Chromosomal anomalies
syndrome
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