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Disease Ontology Browser
cataract 41 (DOID:0110241)
Alliance: disease page
Synonyms: congenital nuclear type cataract 41; CTRCT41
Alt IDs: OMIM:116400, ICD10CM:Q12.0
Definition: A cataract that has_material_basis_in heterozygous mutation in the WFS1 gene on chromosome 4p16.

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 6.15
The Jackson Laboratory