raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:168486

OBSOLETE: Congenital neuronal ceroid lipofuscinosis

inactive · referred to ORPHA:216Neuronal ceroid lipofuscinosis

Synonyms: OBSOLETE: Congenital NCL

Type
Disease
Group
Disorder
Status
inactive
Flag
Obsolete entity

This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Neuronal ceroid lipofuscinosis

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Congenital neuronal ceroid lipofuscinosisOBSOLETE: Congenital NCL
frOBSOLETE : Céroïde-lipofuscinose neuronale congénitaleOBSOLETE : CLN congénitale · OBSOLETE : NCL congénitale
deOBSOLET: Ceroid-Lipofuszinose, neuronale, kongenitaleOBSOLET: CLN10 · OBSOLET: Ceroid-Lipofuszinose, neuronale (CLN10) · OBSOLET: NCL, kongenitale
esOBSOLETO: Lipofuscinosis ceroide neuronal congénitaOBSOLETO: Ceroidolipofuscinosis neuronal congénita · OBSOLETO: LCN congénita · OBSOLETO: NCL congénita
itOBSOLETO: Ceroido lipofuscinosi neuronale congenitaOBSOLETO: NCL congenita
nlOBSOLEET: Congenitale neuronale ceroïdlipofuscinoseOBSOLEET: Congenitale NCL
ptOBSOLETO: Lipofuscinose ceróide neuronal congénita
plNIEAKTUALNE: Wrodzona ceroidolipofuscynoza neuronalnaNIEAKTUALNE: Wrodzona NCL
csNEAKTUÁLNÍ: Vrozená forma neuronální ceroidlipofuscinózyNEAKTUÁLNÍ: Vrozená NCL
ukЗАСТАРІЛО: Вроджений нейрональний цероїдний ліпофусцинозЗАСТАРІЛО: Вроджена НКЛ
zh先天性神经元蜡样脂褐质贮积病先天性NCL
trDoğumsal nöronal seroid lipofuksinozDoğumsal NCL

Definition in:

2

Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

3

Classification

Not placed in any Orphanet classification in this release.

No children.

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