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Disease Ontology Browser
cataract 18 (DOID:0110238)
Alliance: disease page
Synonyms: autosomal recessive congenital cataract 2; cataract 18 autosomal recessive; CATC2; CTRCT18
Alt IDs: OMIM:610019, ICD10CM:Q12.0
Definition: A cataract that has_material_basis_in homozygous mutation in the FYCO1 gene on chromosome 3p21.3.


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
10/10/2017
MGI 6.10
The Jackson Laboratory