ORPHA:404538

X-linked distal hereditary motor neuropathy

Synonyms: X-linked dHMN · X-linked distal spinal muscular atrophy

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

12 of 12 languages

Lang	Name	Synonyms
en	X-linked distal hereditary motor neuropathy	X-linked dHMN · X-linked distal spinal muscular atrophy
fr	Neuropathie motrice distale héréditaire liée à l'X	Amyotrophie spinale distale liée à l'X · dHMN liée à l'X · dSMA liée à l'X
de	Neuropathie, distale hereditäre motorische, X-chromosomale	Spinale Muskelatrophie, distale, X-chromosomale · dHMN, X-chromosomal
es	Neuropatía motora distal hereditaria ligada al cromosoma X	dHMN ligada al cromosoma X
it	Neuropatia motoria ereditaria distale legata all'X	Atrofia muscolare spinale distale legata all'X · dHMN legata all'X
nl	X-gebonden distale erfelijke motorneuropathie	X-gebonden dHMN · X-gebonden distale spinale spieratrofie
pt	Neuropatia motora hereditária distal ligada ao cromossoma X
pl	Dziedziczna dystalna neuropatia ruchowa sprzężona z chromosomem X	dHMN sprzężony z chromosomem X · Dystalny rdzeniowy zanik mięśni sprzężony z chromosomem X
cs	X-vázaná distální hereditární motorická neuropatie	X-vázaná dHMN · X-vázaná distální spinální svalová atrofie
uk	Х-зчеплена спадкова дистальна моторна нейропатія	Х-зчеплений dHMN · Х-зчеплена дистальна спінальна мязова атрофія
zh	X连锁远端遗传性运动神经病	X连锁远端脊髓性肌萎缩
tr	X'e bağlı distal kalıtsal motor nöropati	X'e bağlı dHMN · X'e bağlı distal spinal kas atrofisi

Cross-references

qualifier = Orphanet mapping relation

Source	Code	Qualifier	ICD relation	Validation
MONDO	18451	E		validated
UMLS	C5548214	E		validated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

Classification

Preferential parent (Orphanet linearisation):

ORPHA:98006Rare neurologic disease

Parents in the classifications (1):

ORPHA:53739Distal hereditary motor neuropathy
rare genetic diseases; rare neurological diseases

Children (3):

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/404538
This record as JSON: /data/d/404538.json