raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:307052

Rare genetic parkinsonian disorder

Synonyms: Rare genetic hypokinetic movement disorder

Type
Category
Group
Group of disorders
Status
active

This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enRare genetic parkinsonian disorderRare genetic hypokinetic movement disorder
frSyndrome parkinsonien génétique rareTrouble du mouvement hypokinétique génétique rare
deSeltenes genetisches Parkinson-SyndromSeltene genetische hypokinetische Bewegungsstörung
esTrastorno parkinsoniano genético raroTrastorno del movimiento hipocinético genético raro
itDisturbo parkinsoniano genetico raro
nlZeldzame genetische parkinsonstoornisZeldzame genetische hypokinetische bewegingsstoornis
ptDoença parkinsónica genética rara
plRzadkie zaburzenia parkinsonowskie uwarunkowane genetycznie= en
csVzácné geneticky podmíněné parkinsonské poruchy= en
ukРідкісний генетично обумовлений паркінсонічний розладРідкісний генетичний гіпокінетичний руховий розлад
zh罕见遗传性帕金森病= en
trNadir genetik parkinson hastalığıNadir genetik hipokinetik hareket bozukluğu
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO17660Evalidated
UMLSC5679955Evalidated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

3

Classification

Preferential parent (Orphanet linearisation):

Parents in the classifications (1):

Children (2):

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

0 records

No prevalence record in this release.

6

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

7

Sources for this card