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Summary Literature (0)
DOID:0070353 - cataract 47


Disease Ontology Definition:A cataract that has_material_basis_in heterozygous mutation in the SLC16A12 gene on chromosome 10q23, characterized by progressive juvenile cataract with microcornea.

Synonyms: CTRCT47

Xenbase Genes : slc16a12


OMIM:
OMIM:612018 - CATARACT 47; CTRCT47

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), cataract (is_a)