Weissenbacher-Zweymuller syndrome

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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 Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

:

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0010195 - obsolete Weissenbacher-Zweymuller syndrome

MONDO:0010195 - obsolete Weissenbacher-Zweymuller syndrome

MIM:

MIM:261800 - PIERRE ROBIN SYNDROME; PRBNS

MIM:261800 - PIERRE ROBIN SYNDROME; PRBNS

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): osteochondrodysplasia (is_a)