Disease #00020 (WD (WILSON DISEASE), OMIM:277900)

Official abbreviation WD
Name WILSON DISEASE
OMIM ID 277900
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene ATP7B
Associated tissues -
Disease features -
Remarks -
Date created 2016-07-08 14:44:00 +00:00 (UTC)
Date last edited 2023-06-16 08:38:09 +00:00 (UTC)