raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:51013

OBSOLETE: Melanoma-pancreatic cancer syndrome

inactive · referred to ORPHA:404560Familial atypical multiple mole melanoma syndrome

Type
Disease
Group
Disorder
Status
inactive
Flag
Obsolete entity

This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Familial atypical multiple mole melanoma syndrome

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Melanoma-pancreatic cancer syndrome
frOBSOLETE : Syndrome de mélanome-cancer pancréatique
deOBSOLET: Melanoma-Pankreaskrebs-Syndrom
esOBSOLETO: Síndrome melanoma-tumor pancreático
itOBSOLETO: Sindrome melanoma-tumore pancreatico
nlOBSOLEET: Melanoom - pancreaskanker-syndroom
ptOBSOLETO: Síndrome melanoma-cancro pancreático
plNIEAKTUALNE: Zespól czerniak i rak trzustki
csNEAKTUÁLNÍ: Syndrom zahrnující melanom a rakovinu slinivky břišní
ukЗАСТАРІЛО: Синдром меланоми та раку підшлункової залози
zh弃用:黑色素瘤-胰腺癌综合征
trEski adı: Melanom-pankreas kanseri sendromu
2

Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

3

Classification

Not placed in any Orphanet classification in this release.

No children.

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