All diseases

OMIM ID
208530
OMIM term:
ASPLENIA WITH CARDIOVASCULAR ANOMALIES
Alternative terms:
IVEMARK SYNDROME POLYSPLENIA SYNDROME, INCLUDED
POLYASPLENIA, INCLUDED
HETEROTAXY, VISCEROATRIAL, AUTOSOMAL RECESSIVE, INCLUDED
VAH, AUTOSOMAL RECESSIVE, INCLUDED
(∗) Location:
(†) Associated OMIM genes:
(‡) Associated MGI genes:
Acvr2b   Cfc1  

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