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Summary Literature (0)
DOID:0110247 - cataract 36


Disease Ontology Definition:A cataract that has_material_basis_in homozygous mutation in the TDRD7 gene on chromosome 9q22.33.

Synonyms: autosomal recessive congenital cataract 4, CATC4, CTRCT36

Xenbase Genes : tdrd7

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013484 - cataract 36

MIM:
MIM:613887 - CATARACT 36; CTRCT36

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Disease Hierarchy:Legend: is acataract 36 (0)This image is generated by www.xenbase.org. Please cite Xenbase in your publications.
Parent(s): autosomal recessive disease (is_a), cataract (is_a)