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Disease Ontology Browser
cataract 38 (DOID:0110245)
Alliance: disease page
Synonyms: autosomal recessive congenital cataract 5; CATC5; CTRCT38
Alt IDs: OMIM:614691, ICD10CM:Q12.0
Definition: A cataract that has_material_basis_in homozygous mutation in the AGK gene on chromosome 7q34.

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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Send questions and comments to User Support. 		last database update
04/16/2024
MGI 6.23 		The Jackson Laboratory