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Parkinson disease

MONDO:0005180

Also known as: PD, Parkinson disease, Parkinson's disease, paralysis agitans

MONDO:
MONDO:0005180
Orphanet:
319705
Rare disease494 associated genes

Description

A progressive degenerative disorder of the central nervous system characterized by loss of dopamine producing neurons in the substantia nigra and the presence of Lewy bodies in the substantia nigra and locus coeruleus. Signs and symptoms include tremor which is most pronounced during rest, muscle rigidity, slowing of the voluntary movements, a tendency to fall back, and a mask-like facial expression.

Associated genes

+484 more genes — install the extension to see the full list inline on any page.

External references

Sources: MONDO (CC BY 4.0), Open Targets (CC0), Orphanet (CC BY 4.0).

Not for sole clinical decision-making. Always verify against primary sources.