Stickler syndrome 2

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Summary

Literature (0)

DOID:0080675 - Stickler syndrome 2

Disease Ontology Definition:A Stickler syndrome that has_material_basis_in heterozygous mutation in the COL11A1 gene on chromosome 1p21.

Synonyms:

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

: col11a1

MIM:

MIM:604841 - STICKLER SYNDROME, TYPE II; STL2

MIM:604841 - STICKLER SYNDROME, TYPE II; STL2

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), Stickler syndrome (is_a)