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DOID:14764 - Larsen syndrome
Disease Ontology Definition:An autosomal dominant disease that is characterized by large-joint dislocations and characteristic craniofacial abnormalities.
Synonyms: dominant larsen syndrome,
Echinobase Genes :
MIM:150250 - larsen syndrome; lrs |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
autosomal dominant disease (is_a)