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Autosomal Dominant Parkinson Disease 4 (MONDO:0011562)

A late onset Parkinson disease that has material basis in heterozygous triplication of the alpha-synuclein gene (SNCA) on chromosome 4q22.

Overview

Category

Ontology ID

Internal:12658

Synonyms

autosomal dominant Parkinson disease 4

autosomal dominant Parkinson disease type 4

PARK4

Parkinson disease 4, autosomal dominant

Parkinson disease 4, autosomal dominant Lewy body

autosomal dominant Parkinson's disease 4

Mapped terms

DOID:0060895

GARD:0018475

MEDGEN:381361

MESH:C565324

OMIM:605543

UMLS:C1854182

Child terms

Unknown children.