All diseases

OMIM ID
236100
OMIM term:
HOLOPROSENCEPHALY
Alternative terms:
HOLOPROSENCEPHALY, FAMILIAL ALOBAR
HPE, FAMILIAL; HPEC
ARHINENCEPHALY HOLOPROSENCEPHALY 1, INCLUDED; HPE1, INCLUDED
CYCLOPIA, INCLUDED
DEMYER SEQUENCE, INCLUDED
(∗) Location:
21q22.3  
(†) Associated OMIM genes:
(‡) Associated MGI genes:
Cdon  

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