raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:3229

OBSOLETE: Deafness-peripheral neuropathy-arterial disease syndrome

inactive · referred to ORPHA:90642Rare syndromic genetic deafness

Type
Malformation syndrome
Group
Disorder
Status
inactive
Flag
Obsolete entity

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

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Deafness-peripheral neuropathy-arterial disease syndrome
frOBSOLETE : Syndrome de surdité-neuropathie périphérique-artériopathie
deOBSOLET: Schwerhörigkeit - periphere Neuropathie - Arteriopathie
esOBSOLETO: Síndrome de sordera-neuropatía periférica-enfermedad arterial
itOBSOLETO: Sordità - neuropatia periferica - arteriopatia
nlOBSOLEET: Doofheid - perifere neuropathie - arteriële ziekte-syndroom
ptOBSOLETO: Síndrome de surdez-neuropatia periférica-doença arterial
plNIEAKTUALNE: Gluchota - neuropatia obwodowa - choroba tetnic
csNEAKTUÁLNÍ: Syndrom zahrnující hluchotu, periferní neuropatii a arteriální onemocnění
ukЗАСТАРІЛО: Синдром глухоти-периферичної нейропатії-артеріальної хвороби
zh弃用:耳聋-周围神经病-动脉病综合征
trEski adı: Sağırlık-periferik nöropati-arteriyel hastalık sendromu
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