All diseases

OMIM ID
140000
OMIM term:
HAND-FOOT-UTERUS SYNDROME
Alternative terms:
HFU SYNDROME
HAND-FOOT-GENITAL SYNDROME
HFG SYNDROME
(∗) Location:
7p15.2  
(†) Associated OMIM genes:
HOXA13  
(‡) Associated MGI genes:
Hoxa13  

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