Term Name:	autosomal dominant Robinow syndrome 1
Synonyms:	DRS1
Definition:	A Robinow syndrome characterized by autosomal dominant inheritance of dysmorphic features resembling a fetal face, mesomelic limb shortening, hypoplastic external genitalia in males, and renal and vertebral anomalies that has_material_basis_in heterozygous mutation in the WNT5A gene on chromosome 3p.
Ontology:	Human Disease [DOID:0060766]   ( DOID:0060766 )