All diseases

OMIM ID
101600
OMIM term:
PFEIFFER SYNDROME
Alternative terms:
ACROCEPHALOSYNDACTYLY, TYPE V; ACS5
ACS V
NOACK SYNDROME CRANIOFACIAL-SKELETAL-DERMATOLOGIC DYSPLASIA, INCLUDED
(∗) Location:
10q26.13   8p11.23-p11.22  
(†) Associated OMIM genes:
FGFR1   FGFR2  
(‡) Associated MGI genes:
Fgfr1   Fgfr2  

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* quick link - http://q.sanger.ac.uk/soclv1j5