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DOID:893 - Wilson disease
Disease Ontology Definition:n_a
Synonyms: Cerebral pseudosclerosis, Westphal pseudosclerosis, Westphal-Strumpell syndrome, Wilson's disease, hepatolenticular degeneration,
Echinobase Genes :
MIM:277900 - wilson disease |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
liver disease (is_a),
metal metabolism disorder (is_a)