DISEASES

Disease-gene associations mined from literature

Human genes for Robinow syndrome

Robinow syndrome [DOID:0060254]

A syndrome characterized by mild to moderate short stature due to growth delays after birth, distinctive craniofacial abnormalities, skeletal malformations and genital abnormalities.

Synonyms:  Robinow syndrome,  DOID:0060254,  Robinow disease,  Robinow disorder,  Robinow syndromes ...