All diseases

OMIM ID
180700
OMIM term:
ROBINOW SYNDROME, AUTOSOMAL DOMINANT; DRS
Alternative terms:
ROBINOW DWARFISM
FETAL FACE SYNDROME
ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES
(∗) Location:
3p14.3  
(†) Associated OMIM genes:
WNT5A  
(‡) Associated MGI genes:

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