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Disease Ontology Browser
cataract 22 multiple types (DOID:0110268)
Alliance: disease page
Synonyms: autosomal recessive congenital nuclear cataract 2; CATCN2; CTRCT22
Alt IDs: OMIM:609741, ICD10CM:Q12.0
Definition: A cataract that has_material_basis_in heterozygous or homozygous mutation in the beta-B3 crystallin gene (CRYBB3) on chromosome 22q11.


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
11/07/2017
MGI 6.11
The Jackson Laboratory