All diseases

OMIM ID
101200
OMIM term:
APERT SYNDROME
Alternative terms:
ACROCEPHALOSYNDACTYLY, TYPE I; ACS1
ACS I APERT-CROUZON DISEASE, INCLUDED
ACROCEPHALOSYNDACTYLY, TYPE II, INCLUDED
ACS II, INCLUDED
VOGT CEPHALODACTYLY, INCLUDED
(∗) Location:
10q26.13  
(†) Associated OMIM genes:
FGFR2  
(‡) Associated MGI genes:
Fgfr2  

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* quick link - http://q.sanger.ac.uk/3uq228tx