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Disease Ontology Browser
cataract 17 multiple types (DOID:0110270)
Alliance: disease page
Synonyms: autosomal recessive congenital nuclear cataract 3; CATCN3; CTRCT17
Alt IDs: OMIM:611544, ICD10CM:Q12.0
Definition: A cataract that has_material_basis_in heterozygous or homozygous mutation in the beta-B1 crystallin gene (CRYBB1) on chromosome 22q12.

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
MGI 6.21
The Jackson Laboratory