Rare parkinsonian syndrome

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Rare parkinsonian syndrome due to genetic neurodegenerative disease

ORPHA:307055Category

What it is

Orphanet has not published a description for this disease yet. The identifiers, classification and cross-references below are still current.

Key facts

Classified as
Category

Genes reported in subtypes

ATP6AP2CMPK2DCTN1DNAJC13DNAJC6EIF4G1FBXO7GBA1GIGYF2HTRA2JAM2LRRK2MYORGNAA60PARK7PDE8BPDGFBPDGFRBPINK1PLA2G6PODXLPRKNPRKRARAB39BRRP12SLC20A2SLC30A10SLC6A3SNCASYNJ1TAF1UCHL1VPS13CVPS35WARS2XPR1

Orphanet records these genes on 14 more specific entries under this disorder, not on this entry itself:

Atypical juvenile parkinsonismAutosomal dominant striatal neurodegenerationBilateral striopallidodentate calcinosisCirrhosis-dystonia-polycythemia-hypermanganesemia syndromeDystonia 16Early-onset parkinsonism-intellectual disability syndromeHereditary late-onset Parkinson diseaseInfantile dystonia-parkinsonismParkinsonian-pyramidal syndromePerry syndromePLA2G6-related neurodegeneration, adult-onsetX-linked dystonia-parkinsonismX-linked parkinsonism-spasticity syndromeYoung-onset Parkinson disease

A well-studied disease is usually split into subtypes, and the gene is curated on whichever one the evidence belongs to. Open a subtype to see which gene goes with it.

Cross-references

MONDO 17661UMLS C5681055

Orphadata Science: Free access data from Orphanet. © INSERM 1999. Data version 2026-06-23. Available under CC BY 4.0. This is a reference, not medical advice.

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