All diseases

OMIM ID
209880
OMIM term:
CENTRAL HYPOVENTILATION SYNDROME, CONGENITAL; CCHS
Alternative terms:
AUTONOMIC CONTROL, CONGENITAL FAILURE OF ONDINE CURSE, CONGENITAL ONDINE-HIRSCHSPRUNG DISEASE, INCLUDED; OHD, INCLUDED
CCHS WITH HIRSCHSPRUNG DISEASE, INCLUDED
HADDAD SYNDROME, INCLUDED
(∗) Location:
10q11.21   11p14.1   12q23.2   20q13.32   4p13   5p13.2  
(†) Associated OMIM genes:
ASCL1   BDNF   EDN3   GDNF   PHOX2B   RET  
(‡) Associated MGI genes:
Phox2b   Tlx3  

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