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

MVZ für Humangenetik Regensburg

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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)