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 ...