raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:2033

OBSOLETE: Multifocal muscular fibrosis-obstructed vessels syndrome

inactive · referred to ORPHA:98006Rare neurologic disease

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 Rare neurologic disease

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Multifocal muscular fibrosis-obstructed vessels syndrome
frOBSOLETE : Syndrome de fibrose musculaire multifocale-vaisseaux obstrués
deOBSOLET: Muskelfibrose, multifokale, mit Gefässverschluss
esOBSOLETO: Síndrome de fibrosis muscular multifocal-vasos obstruidos
itOBSOLETO: Fibrosi muscolare multifocale - ostruzione dei vasi
nlOBSOLEET: Multifocale spierfibrose - verstopte bloedvaten-syndroom
ptOBSOLETO: Síndrome de fibrose muscular multifocal-oclusão dos vasos
plNIEAKTUALNE: Wieloogniskowe wlóknienie miesni - zwezenie naczyn
csNEAKTUÁLNÍ: Syndrom zahrnující multifokální svalovou fibrózu a obstrukci cév
ukЗАСТАРІЛО: Синдром мультифокального мязевого фіброзу-обструкції судин
zh弃用:多灶性肌肉纤维化-血管阻塞综合征
trEski adı: Multifokal musküler fibroz ile tıkalı damar 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