raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:300515

Rare nail tumor

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 nail tumor
frTumeur rare des onglesTumeur unguéale rare
deNageltumor, seltener
esTumor raro de las uñas
itTumore raro delle unghie
nlZeldzame nageltumor
ptTumor raro das unhas
plRzadki guz paznokcia
csVzácné nádory nehtů
ukРідкісна пухлина нігтя
zh罕见的指甲肿瘤
trNadir tırnak tümörü
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO17588Evalidated
UMLSC5681082Evalidated

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 (2):

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