All diseases

OMIM ID
142623
OMIM term:
HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 1; HSCR1
Alternative terms:
HIRSCHSPRUNG DISEASE; HSCR
AGANGLIONIC MEGACOLON
MEGACOLON, AGANGLIONIC; MGC
(∗) Location:
10q11.21  
(†) Associated OMIM genes:
RET  
(‡) Associated MGI genes:
Edn3   Ednrb   Gdnf   Gfra1   Gfra2   Ihh   Ret   Sox10   Spry2  

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