cataract 48 Disease Ontology Browser

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Disease Ontology Browser

cataract 48 (DOID:0070354)
Alliance: disease page
Synonyms: CTRCT48
Alt IDs: OMIM:618415
Definition: A cataract that has_material_basis_in homozygous mutation in the DNMBP gene on chromosome 10q24 and is characterized by infantile or early-childhood cataracts and visual impairment.

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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