ORPHA:700143

X-linked distal myopathy

Type: Category
Group: Group of disorders
Status: active

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.

Names in Orphadata languages

9 of 12 languages

Lang	Name	Synonyms
en	X-linked distal myopathy
fr	Myopathie distale liée à l'X
de	X-chromosomale distale Myopathie
es	Miopatía distal ligada al cromosoma X
it	Miopatia distale legata all'X
nl	X-gebonden distale myopathie
pt	X-linked distal myopathy
pl	X-linked distal myopathy
cs	X-linked distal myopathy

Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

Classification

Preferential parent (Orphanet linearisation):

ORPHA:98006Rare neurologic disease

Parents in the classifications (1):

ORPHA:599Distal myopathy
rare genetic diseases; rare neurological diseases

Children (1):

ORPHA:700163SMPX-related distal myopathy

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/700143
This record as JSON: /data/d/700143.json