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Summary Literature (0)
DOID:4258 - Weissenbacher-Zweymuller syndrome

Disease Ontology Definition:An osteochondrodysplasia that results_in shortened long bones and distinct facial abnormalities.

Synonyms: Piere-Robin syndrome, Pierre Robin Malformation

Xenbase Genes :

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010195 - obsolete Weissenbacher-Zweymuller syndrome

MIM:
MIM:261800 - PIERRE ROBIN SYNDROME; PRBNS

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view
Parent(s): osteochondrodysplasia (is_a)