raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:211247

Rare capillary 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.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enRare capillary malformation
frMalformation capillaire rare
deKapilläre Fehlbildung, seltene
esMalformación capilar rara
itMalformazione capillare
nlCapillaire malformatie
ptMalformação capilar
plMalformacja włośniczkowa
csVzácná kapilární malformace
ukРідкісна капілярна мальформація
zh罕见毛细血管畸形
trNadir kılcal malformasyon
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO16231Evalidated
UMLSC5680860Evalidated

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 (8):

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