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DOID:0110272 - cataract 40
Disease Ontology Definition:A cataract that has_material_basis_in mutation in the NHS gene on chromosome Xp22.
Synonyms: CTRCT40, cataract 40 X-linked, cataract 40 with or without microcornea,
Xenbase Genes : nhs
MONDO:0010544 - cataract 40 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
X-linked monogenic disease (is_a),
cataract (is_a)