raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:228340

OBSOLETE: CLN4A disease

inactive · referred to ORPHA:228363CLN6 disease

Type
Etiological subtype
Group
Subtype of disorder
Status
inactive
Flag
Obsolete entity

This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using CLN6 disease

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: CLN4A disease
frOBSOLETE : Maladie CLN4A
deOBSOLET: CLN4A-Krankheit
esOBSOLETO: Enfermedad CLN4A
itOBSOLETO: Malattia CLN4A
nlOBSOLEET: CLN4A-ziekte
ptOBSOLETO: Doença CLN4A
plNIEAKTUALNE: Choroba CLN4A
csNEAKTUÁLNÍ: Neuronální ceroidlipofuscinosa, typ 4
ukЗАСТАРІЛО: Хвороба CLN4A
zh神经元蜡样脂褐质沉积症4A型
trCLN4A hastalığı
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