GenTIGSA Gene Database on Rare Genetic Disorders
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Wilson Disease  
Disease Aliases (52)

Cerebral pseudoscleroses

Cerebral pseudosclerosis

Copper storage disease

Copper storage diseases

Degeneration syndrome, hepatolenticular

Degeneration syndromes, hepatolenticular

Degeneration, hepatocerebral

Degeneration, hepatolenticular

Degeneration, neurohepatic

Degeneration, progressive lenticular

Degenerations, hepatocerebral

Degenerations, neurohepatic

Disease, copper storage

Diseases, copper storage

Diseases, hepato-neurologic wilson

Diseases, kinnier-wilson

Hepatolenticular degeneration

Hepatic form of wilson disease

Hepato neurologic wilson disease

Hepato-neurologic wilson disease

Hepato-neurologic wilson diseases

Hepatocerebral degeneration

Hepatocerebral degenerations

Hepatolenticular degeneration syndrome

Hepatolenticular degeneration syndromes

Kinnier wilson disease

Kinnier-wilson disease

Kinnier-wilson diseases

Lenticular degeneration, progressive

Neurohepatic degeneration

Neurohepatic degenerations

Progressive lenticular degeneration

Pseudoscleroses, cerebral

Pseudosclerosis

Pseudosclerosis, cerebral

Storage disease, copper

Storage diseases, copper

Syndrome, hepatolenticular degeneration

Syndromes, hepatolenticular degeneration

Wd

Wd - wilson's disease

Wnd

Westphal strumpell syndrome

Westphal pseudosclerosis

Westphal-strumpell syndrome

Westphal-strumpell syndromes

Wilson disease

Wilson disease, hepatic form

Wilson disease, hepato-neurologic

Wilson diseases, hepato-neurologic

Wilson's disease

Wilsons disease

Associated Genes (1)
 

NCBI-RefSeq:  ATP7B   (ATPase copper transporting beta)

External Links:  gnomAD browser   Ensembl   GeneCards

 


Cross-references of Wilson disease OMIM GARD Orphanet NCBI-GTR NCBI-MedGen MalaCards      MeSH Annotations