ORPHA:269194

Central nervous system cystic malformation

Type: Category
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.

Names in Orphadata languages

12 of 12 languages

Lang	Name	Synonyms
en	Central nervous system cystic malformation
fr	Malformation kystique du système nerveux central
de	Zystische Fehlbildung des Zentralnervensystems
es	Malformación quística del sistema nervioso central
it	Malformazione cistica del sistema nervoso centrale
nl	Cysteuze malformatie van centraal zenuwstelsel
pt	Malformação quística do sistema nervoso central
pl	Malformacja torbielowata centralnego układu nerwowego
cs	Cystická malformace centrálního nervového systému
uk	Кістозна мальформація центральної нервової системи
zh	中枢神经系统囊性畸形
tr	Merkezi sinir sistemi kistik malformasyonu

Cross-references

qualifier = Orphanet mapping relation

Source	Code	Qualifier	ICD relation	Validation
MONDO	17104	E		validated
UMLS	C5680777	E		validated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

Classification

Preferential parent (Orphanet linearisation):

ORPHA:93890Rare developmental defect during embryogenesis

Parents in the classifications (1):

ORPHA:729560Forebrain malformation
rare developmental anomalies during embryogenesis; rare neurological diseases

Children (2):

Codes that Orphanet moved or referred to this one:

ORPHA:98520OBSOLETE: Cystic malformation of the posterior fossa referred to · inactive

Genes

0 direct

Orphanet records no gene directly on this code.

Prevalence and incidence

0 records

No prevalence record in this release.

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

Sources for this card

Orphanet page: orpha.net/en/disease/detail/269194
This record as JSON: /data/d/269194.json