ORPHA:730390

Genetic posterior fossa 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

9 of 12 languages

Lang	Name	Synonyms
en	Genetic posterior fossa cystic malformation
fr	Malformation kystique génétique de la fosse postérieure
de	Zystische Fehlbildung der hinteren Schädelgrube, genetisch bedingte
es	Malformación quística genética de la fosa posterior
it	Malformazione cistica genetica della fossa posteriore
nl	Genetische cysteuze malformatie van fossa cranialis posterior	Genetische cysteuze malformatie van achterste schedelgroeve
pt	Genetic posterior fossa cystic malformation
pl	Genetic posterior fossa cystic malformation
cs	Genetic posterior fossa cystic malformation

Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

Classification

Preferential parent (Orphanet linearisation):

ORPHA:93890Rare developmental defect during embryogenesis

Parents in the classifications (1):

ORPHA:730382Genetic midbrain-hindbrain malformation
rare genetic diseases

Children (2):

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/730390
This record as JSON: /data/d/730390.json