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Summary Literature (1)
DOID:0060254 - Robinow syndrome

Disease Ontology Definition: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 dwarfism, acral dysostosis with facial and genital abnormalities, fetal face syndrome,

Xenbase Genes : dvl1, ror2, dvl3, nxn, wnt5a

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0019978 - Robinow syndrome


Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal genetic disease (is_a), syndrome (is_a)