cataract 47 Disease Ontology Browser

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Disease Ontology Browser

cataract 47 (DOID:0070353)
Alliance: disease page
Synonyms: CTRCT47
Alt IDs: OMIM:612018
Definition: A cataract that has_material_basis_in heterozygous mutation in the SLC16A12 gene on chromosome 10q23, characterized by progressive juvenile cataract with microcornea.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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