All diseases

OMIM ID
180849
OMIM term:
RUBINSTEIN-TAYBI SYNDROME 1; RSTS1
Alternative terms:
RUBINSTEIN SYNDROME
BROAD THUMBS AND GREAT TOES, CHARACTERISTIC FACIES, AND MENTAL RETARDATION
BROAD THUMB-HALLUX SYNDROME
(∗) Location:
16p13.3  
(†) Associated OMIM genes:
CREBBP  
(‡) Associated MGI genes:
Crebbp  

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