All diseases

OMIM ID
101400
OMIM term:
SAETHRE-CHOTZEN SYNDROME; SCS
Alternative terms:
ACROCEPHALOSYNDACTYLY, TYPE III; ACS3
ACS III
CHOTZEN SYNDROME
ACROCEPHALY, SKULL ASYMMETRY, AND MILD SYNDACTYLY SAETHRE-CHOTZEN SYNDROME WITH EYELID ANOMALIES, INCLUDED
BLEPHAROPHIMOSIS, EPICANTHUS INVERSUS, AND PTOSIS 3, FORMERLY, INCLUDED; BPES3, FORMERLY, INCLUDED
(∗) Location:
10q26.13   7p21.1  
(†) Associated OMIM genes:
FGFR2   TWIST1  
(‡) Associated MGI genes:
Twist1  

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