Term Name:	Robinow syndrome
Synonyms:	acral dysostosis with facial and genital abnormalities, fetal face syndrome, Robinow dwarfism
Definition:	A syndrome characterized by mild to moderate short stature due to growth delays after birth, distinctive craniofacial abnormalities, skeletal malformations and genital abnormalities.
Ontology:	Human Disease [DOID:0060254] ( DOID:0060254 )

Relationships

is a type of:	autosomal genetic disease syndrome
has subtype:	autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal recessive Robinow syndrome autosomal recessive Robinow syndrome 2