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Summary Literature (0)
DOID:14764 - Larsen syndrome

Disease Ontology Definition:A syndrome that is characterized by autosomal dominant inheritance of large-joint dislocations and characteristic craniofacial abnormalities.

Synonyms: dominant larsen syndrome

Xenbase Genes : flnb

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0007875 - Larsen syndrome

MIM:
MIM:150250 - LARSEN SYNDROME; LRS

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

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