raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:363629

OBSOLETE: GMPPB-related congenital muscular dystrophy

inactive · referred to ORPHA:370953Congenital muscular dystrophy due to dystroglycanopathy

Synonyms: OBSOLETE: GMPPB-related CMD

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 Congenital muscular dystrophy due to dystroglycanopathy

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: GMPPB-related congenital muscular dystrophyOBSOLETE: GMPPB-related CMD
frOBSOLETE : Dystrophie musculaire congénitale liée à GMPPBOBSOLETE : DMC liée à GMBPP
deOBSOLET: Muskeldystrophie, kongenitale, GMPPB-bedingteOBSOLET: GMPPB-assoziierte CMD
esOBSOLETO: Distrofia muscular congénita asociada a GMPPBOBSOLETO: DMC asociada a GMPPB
itOBSOLETO: Distrofia muscolare congenita GMPPB-correlataOBSOLETO: CMD GMPPB-correlata
nlOBSOLEET: GMPPB-gerelateerde congenitale spierdystrofieOBSOLEET: GMPPB-gerelateerde CMD
ptOBSOLETO: Distrofia muscular congénita GMPPB-relacionada
plNIEAKTUALNE: Wrodzona dystrofia miesniowa zwiazana z GMPPBNIEAKTUALNE: CMD związana z GMPPB
csNEAKTUÁLNÍ: GMPPB-vázaná vrozená svalová dystrofie= en
ukЗАСТАРІЛО: Вроджена мязова дистрофія, повязана з GMPPBЗАСТАРІЛО: CMD, повязаний з GMPPB
zh弃用:GMPPB基因相关先天性肌营养不良GMPPB基因相关CMD
trEski adı: GMPPB-ilişkili Doğumsal musküler distrofiGMPPB-ilişkili CMD
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