cataract 15 multiple types

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Summary

Literature (0)

DOID:0110251 - cataract 15 multiple types

Disease Ontology Definition:A cataract that has_material_basis_in heterozygous mutation in the MIP gene on chromosome 12q13.

Synonyms: CTRCT15

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

: mip

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014110 - cataract 15 multiple types

MONDO:0014110 - cataract 15 multiple types

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), cataract (is_a)