raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:587

Muir-Torre syndrome

inactive · moved to ORPHA:144Lynch syndrome

Synonyms: Multiple keratoacanthoma, Muir-Torre type

Type
Disease
Group
Disorder
Status
inactive
Flag
Deprecated entity

This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Lynch syndrome

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enMuir-Torre syndromeMultiple keratoacanthoma, Muir-Torre type
frSyndrome de Muir-TorreKératoacanthome multiple de Muir-Torre
deMuir-Torre-Syndrom
esSíndrome de Muir-Torre
itSindrome di Muir-Torre
nlSyndroom van Muir-TorreMeervoudig keratoacanthoom, Muir-Torre-type
ptSíndrome Muir-Torre
plZespół Muira i TorregoRogowiak kolczystokomórkowy typu Muira i Torrego
csTorrého-Muirův syndromMnohočetné keratoakantomy, Muirův-Torrého typ · Torré-Muirův syndrom · Mnohočetné keratoakantomy, Muir-Torrého typ
ukСиндром Мюїр-ТорреМножинна кератоакантома, тип Мюїр-Торре
zhMuir-Torre综合征多发性角化棘皮瘤,Muir-Torre型
trMuir-Torre sendromuÇoklu keratoakantom, Muir-Torre tipi
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
OMIM158320Evalidated
MeSHD055653Evalidated
UMLSC1321489Evalidated
GARD6821Evalidated
MedDRA10063042Evalidated

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

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