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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 Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
12/05/2017
MGI 6.11
The Jackson Laboratory