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Disease Ontology Browser
cataract 39 multiple types (DOID:0110236)
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 Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
03/21/2017
MGI 6.08
The Jackson Laboratory