All diseases

OMIM ID
606217
OMIM term:
ATRIOVENTRICULAR SEPTAL DEFECT, SUSCEPTIBILITY TO, 2; AVSD2 ATRIOVENTRICULAR SEPTAL DEFECT, PARTIAL, WITH HETEROTAXY SYNDROME, INCLUDED
Alternative terms:

(∗) Location:
3p25.3  
(†) Associated OMIM genes:
CRELD1  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/85xcephg