raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:251896

Choroid plexus tumor

Type
Clinical group
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.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enChoroid plexus tumor
frTumeur des plexus choroïdes
deChoroidplexustumor
esTumor del plexo coroideo
itTumore del plesso corioideo
nlTumor van plexus choroideusPlexus choroideus-tumor
ptTumor do plexo coróide
plGuz splotu naczyniówkowego
csNádor choroidálního plexu
ukПухлина судинного сплетення
zh脉络丛瘤
trKoroid pleksus tümörü
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
ICD-112A00.22Especificvalidated
MONDO0016717Evalidated
MONDO16717Evalidated
MeSHD016545Evalidated
UMLSC0085138Evalidated

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

3

Classification

Preferential parent (Orphanet linearisation):

Parents in the classifications (1):

Children (3):

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

1 record
TypeClassValueAreaQualificationValidationSource
Annual incidence<1 / 1 000 0000.05 / 100 000United StatesValue and classValidatedCentral Brain Tumor OTHERistry of the United States 2010-2014[OTHER]_29117289[PMID]

Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.

6

HPO phenotypes

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

7

Sources for this card