raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:329303

PLA2G6-related neurodegeneration

Synonyms: PLA2G6-associated neurodegeneration · PLAN

Type
Clinical group
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
enPLA2G6-related neurodegenerationPLA2G6-associated neurodegeneration · PLAN
frNeurodégénérescence associée à PLA2G6PLAN
dePLA2G6-assoziierte NeurodegenerationPLAN
esNeurodegeneración asociada al gen PLA2G6PLAN
itNeurodegenerazione correlata a PLA2G6Neurodegenerazione associata a PLA2G6 · PLAN
nlPLA2G6-gerelateerde neurodegeneratiePLAN · PLA2G6-geassocieerde neurodegeneratie
ptNeurodegenerescência associada a PLA2G6
plNeurodegeneracja związana z plA2G6plAN
csNeurodegenerace spojená s fosfolipázou A2 s mutací PLA2G6 genuPLAN
ukНейродегенерація, асоційована з PLA2G6PLAN
zhPLA2G6基因相关神经退行性变PLAN
trPLA2G6 -ilişkili nörodejenerasyonPLAN
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO0017998Evalidated
MONDO17998Evalidated

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 (2):

Children (3):

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