raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:715353

Isolated reticulated capillary malformation

Synonyms: Isolated telangiectatic capillary malformation

Type
Morphological anomaly
Group
Disorder
Inheritance
Not applicable
Age of onset
Antenatal, Infancy, Neonatal
Status
active

Orphadata ships no English definition for this code.

1

Names in Orphadata languages

9 of 12 languages
LangNameSynonyms
enIsolated reticulated capillary malformationIsolated telangiectatic capillary malformation
frMalformation capillaire réticulaire isoléeMalformation capillaire télangiectasique isolée
deIsolierte netzartige kapilläre FehlbildungIsolierte teleangiektatische kapilläre Malformation
esMalformación capilar reticular aisladaMalformación capilar telangiectásica aislada
itMalformazione capillare reticolata isolataMalformazione capillare telangectasica isolata
nlGeïsoleerde reticulaire capillaire malformatieGeïsoleerde teleangiëctatische capillaire malformatie
ptIsolated reticulated capillary malformation
plIzolowana malformacja naczyń włosowatych siateczkowatych= en
csIsolated reticulated capillary malformation= en
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
ICD-10Q27.8NTBTattributedvalidated

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):

No children.

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

1 record
TypeClassValueAreaQualificationValidationSource
Point prevalence<1 / 1 000 000—WorldwideClass onlyValidatedORPHANET

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