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Disease Ontology Browser
cataract 13 with adult i phenotype (DOID:0110242)
Alliance: disease page
Synonyms: CTRCT13
Alt IDs: OMIM:116700, ICD10CM:Q12.0
Definition: A cataract that has_material_basis_in homozygous or compound heterozygous mutation in the GCNT2 gene on chromosome 6p24.

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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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MGI 6.12
The Jackson Laboratory