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DO Term : Wilson disease [DOID:893] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A metal metabolism disease that is characterized by excess copper stored in various body tissues, particularly the liver, brain, and corneas of the eyes.

synonyms:
Cerebral pseudosclerosis,
MESH:D006527,
OMIM:277900,
NCI:C84756,
Westphal pseudosclerosis,
ICD10CM:E83.01,
Westphal-Strumpell syndrome,
SNOMEDCT_US_2023_03_01:88518009,
UMLS_CUI:C0019202,
277900,
Wilson's disease,
GARD:7893,
hepatolenticular degeneration

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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