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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.


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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last database update
06/23/2022
MGI 6.20
The Jackson Laboratory