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Summary Literature (0)
DOID:0080046 - Stickler syndrome

Disease Ontology Definition:A syndrome that is characterized by a distinctive facial appearance, eye abnormalities, hearing loss, and joint problems.

Synonyms:

Xenbase Genes : col11a2, col2a1, col11a1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0019354 - Stickler syndrome


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

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