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Disease Ontology Browser
cataract 35 (DOID:0110261)
Alliance: disease page
Synonyms: autosomal recessive congenital nuclear cataract 1; cataract 35, congenital nuclear; CATCN1; CTRCT35
Alt IDs: OMIM:609376, ICD10CM:Q12.0
Definition: A cataract that has_material_basis_in variation in the region 19q13.

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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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Send questions and comments to User Support. 		last database update
12/17/2024
MGI 6.24 		The Jackson Laboratory