All diseases

OMIM ID
142340
OMIM term:
DIAPHRAGMATIC HERNIA, CONGENITAL
Alternative terms:
DIH
HERNIA, CONGENITAL DIAPHRAGMATIC; HCD; CDH
DIAPHRAGMATIC DEFECT, CONGENITAL
DIAPHRAGM, UNILATERAL AGENESIS OF
HEMIDIAPHRAGM, AGENESIS OF DIAPHRAGMATIC HERNIA 1, INCLUDED; DIH1, INCLUDED
DIAPHRAGM, COMPLETE AGENESIS OF, INCLUDED
(∗) Location:
15q26.1  
(†) Associated OMIM genes:
(‡) Associated MGI genes:
Pdgfra   Slit3   Zfpm2  

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