raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:228157

Marburg acute multiple sclerosis

Synonyms: Acute multiple sclerosis, Marburg type · Acute multiple sclerosis, Marburg variant

Type
Disease
Group
Disorder
Inheritance
Multigenic/multifactorial
Age of onset
Adult
Status
active

Marburg acute multiple sclerosis is a rare variant of multiple sclerosis characterized by a rapidly progressive, aggressive form of multiple sclerosis with numerous large multifocal demyelinating lesions in deep white matter on cerebral MRI that usually leads to severe disability or death within weeks to months without remission. A relapsing form of multiple sclerosis is observed in surviving patients.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enMarburg acute multiple sclerosisAcute multiple sclerosis, Marburg type · Acute multiple sclerosis, Marburg variant
frSclérose en plaques aiguë de MarburgSEP aiguë de Marburg · Sclérose de Marburg
deAkute multiple Sklerose MarburgMarburg-Variante der akuten multiplen Sklerose · Multiple Sklerose, akute, Marburg-Variante
esEsclerosis múltiple aguda de MarburgEsclerosis múltiple aguda tipo Marburg · Esclerosis múltiple aguda variante Marburg
itSclerosi multipla acuta di MarburgSclerosi multipla acuta, tipo Marburg · Sclerosi multipla acuta, variante Marburg
nlAcute multipele sclerose van MarburgAcute multipele sclerose, Marburg-type · Acute multipele sclerose, Marburg-variant
ptEsclerose múltipla aguda de Marburg
plPostać Marburga stwardnienia rozsianegoPostać ostra stwardnienia rozsianego, typ Marburga · Postać ostra stwardnienia rozsianego, wariant Marburga
csMarburgova akutní roztroušená sklerózaAkutní roztroušená skleróza, Marburgova varianta · Akutní roztroušená skleróza, Marburgův typ
ukМарбурзький гострий розсіяний склерозГострий розсіяний склероз, марбурзький тип · Гострий розсіяний склероз, марбурзький варіант
zhMarburg急性多发性硬化Marburg变体型急性多发性硬化
trMarburg akut çoklu sklerozAkut çoklu skleroz, Marburg tipi · Akut çoklu skleroz, Marburg varyantı

Definition in:

2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
ICD-10G35NTBTattributedvalidated
ICD-118A4YNTBTindexvalidated
MONDO0016429Evalidated
UMLSC4707723Evalidated

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 prevalenceUnknown—WorldwideClass onlyNot yet validatedORPHANET

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