raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:269557

OBSOLETE: Genetic posterior fossa malformation

inactive · referred to ORPHA:183506Genetic central 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 Genetic central nervous system malformation

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Genetic posterior fossa malformation
frOBSOLETE : Malformation génétique de la fosse postérieure
deOBSOLET: Fehlbildung der hinteren Schädelgrube, genetisch bedingte
esOBSOLETO: Malformación genética de la fosa posterior
itOBSOLETO: Malformazione genetica della fossa posteriore
nlOBSOLEET: Genetische malformatie van fossa posterior
ptOBSOLETO: Malformação da fossa posterior genética
plNIEAKTUALNE: Malformacja dołu tylnego czaszki uwarunkowana genetycznie
csNEAKTUÁLNÍ: Geneticky podmíněné malformace zadní jámy
ukГенетично обумовлена вада розвитку задньої черепної ямки
zh遗传性后颅窝畸形
trGenetik posterior fossa malformasyonu
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Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

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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.

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Sources for this card