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Disease Ontology Browser
cataract 39 multiple types (DOID:0110236)
Alliance: disease page
Synonyms: autosomal dominant cataract 39 multiple types; CTRCT39
Alt IDs: OMIM:615188, ICD10CM:Q12.0
Definition: A cataract that has_material_basis_in heterozygous mutation in the CRYGB gene on chromosome 2q34.

Disease References using Mouse Models (3)

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 6.17
The Jackson Laboratory