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Disease Ontology Browser
cataract 9 multiple types (DOID:0110266)
Alliance: disease page
Synonyms: autosomal recessive congenital cataract 1; cataract 9 multiple types with or without microcornea; CATC1; CTRCT9
Alt IDs: OMIM:604219, ICD10CM:Q12.0
Definition: A cataract that has_material_basis_in autosomal recessive or autosomal dominant inheritance of heterozygous or homozygous mutation in the CRYAA gene, which encodes alpha-A-crystallin, on chromosome 21q22.

Disease References using Mouse Models (6)

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
09/27/2022
MGI 6.21
The Jackson Laboratory