All diseases

OMIM ID
192430
OMIM term:
VELOCARDIOFACIAL SYNDROME
Alternative terms:
CHROMOSOME 22q11.2 DELETION SYNDROME
VCF SYNDROME; VCFS
SHPRINTZEN VCF SYNDROME
(∗) Location:
22q11.21  
(†) Associated OMIM genes:
TBX1  
(‡) Associated MGI genes:
Chrd   Crkl   Ednra   Tbx1  

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* quick link - http://q.sanger.ac.uk/ste9ow86