All diseases

OMIM ID
218040
OMIM term:
COSTELLO SYNDROME
Alternative terms:
FACIOCUTANEOSKELETAL SYNDROME
FCS SYNDROME MYOPATHY, CONGENITAL, WITH EXCESS OF MUSCLE SPINDLES, INCLUDED; CMEMS, INCLUDED
(∗) Location:
11p15.5  
(†) Associated OMIM genes:
HRAS  
(‡) Associated MGI genes:
Hras1  

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