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DOID:0110261 - cataract 35
Disease Ontology Definition:A cataract that has_material_basis_in variation in the region 19q13.
Synonyms: CATCN1, CTRCT35, autosomal recessive congenital nuclear cataract 1, cataract 35, congenital nuclear,
Xenbase Genes :
MONDO:0012260 - cataract 35 |
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)