ORPHA:98469

OBSOLETE: Congenital muscular dystrophy due to glycosyltransferase anomaly

inactive · referred to ORPHA:97242Congenital muscular dystrophy

Type: Category
Group: Group of disorders
Status: inactive
Flag: Obsolete entity

This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.<br/><br/>Instead, consider using Congenital muscular dystrophy

Names in Orphadata languages

12 of 12 languages

Lang	Name	Synonyms
en	OBSOLETE: Congenital muscular dystrophy due to glycosyltransferase anomaly
fr	OBSOLETE : Dystrophie musculaire congénitale par anomalie de la glycosyltransférase
de	OBSOLET: Muskeldystrophie, kongenitale, durch Glykosyltransferase-Anomalie
es	OBSOLETO: Distrofia muscular congénita por una anomalía de la glicosiltransferasa
it	OBSOLETO: Distrofia muscolare congenita da anomalia delle glicosiltransferasi
nl	OBSOLEET: Congenitale spierdystrofie door glycosyltransferaseanomalie
pt	OBSOLETO: Distrofia muscular congénita por anomalia da glicosiltransferase
pl	NIEAKTUALNE: Wrodzona dystrofia miesniowa z powodu anomalii glikozylotransferazy
cs	NEAKTUÁLNÍ: Vrozená svalová dystrofie způsobená anomálií glykosyltransferázy
uk	ЗАСТАРІЛО: Вроджена мязова дистрофія внаслідок аномалії глікозилтрансферази
zh	弃用：糖基转移酶异常所致先天性肌营养不良
tr	Eski adı: Glikosiltransferaz anomalisine bağlı doğumsal kas distrofisi

Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

Classification

Not placed in any Orphanet classification in this release.

No children.

Genes

0 direct

Orphanet records no gene directly on this code.

Prevalence and incidence

0 records

No prevalence record in this release.

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

Sources for this card

Orphanet page: orpha.net/en/disease/detail/98469
This record as JSON: /data/d/98469.json