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Summary Literature (0)
DOID:0110262 - cataract 45

Disease Ontology Definition:A cataract that has_material_basis_in homozygous mutation in the SIPA1L3 gene on chromosome 19q13.

Synonyms: CTRCT45

Xenbase Genes :

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014799 - cataract 45


Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal recessive disease (is_a), cataract (is_a)