raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:108989

OBSOLETE: Non-syndromic central nervous system malformation

inactive · referred to ORPHA:98044Central nervous system malformation

Type
Category
Group
Group of disorders
Status
inactive
Flag
Obsolete entity

This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>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.<br/><br/>Instead, consider using Central nervous system malformation

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Non-syndromic central nervous system malformation
frOBSOLETE : Malformation non syndromique du système nerveux central
deOBSOLET: Nicht-syndromale Fehlbildung des Zentralnervensystems
esOBSOLETO: Malformación no-sindrómica del sistema nervioso central
itOBSOLETO: Malformazione non sindromica del sistema nervoso centrale
nlOBSOLEET: Niet-syndromale malformatie van centraal zenuwstelsel
ptOBSOLETO: Malformação do sistema nervoso central não-sindromática
plNIEAKTUALNE: Niesyndromiczna malformacja centralnego układu nerwowego
csNEAKTUÁLNÍ: Nesyndromické malformace centrálního nervového systému
ukНесиндромальні вади розвитку центральної нервової системи
zh非综合征性中枢神经系统畸形
trSendromik olmayan merkezi sinir sistemi malformasyonu
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