ORPHA:476109

Axonal hereditary motor and sensory neuropathy

Synonyms: Axonal HMSN

Type: Clinical group
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	Axonal hereditary motor and sensory neuropathy	Axonal HMSN
fr	Neuropathie sensitivo-motrice héréditaire axonale	HMSN axonale · NSMH axonale
de	Axonale hereditäre motorisch-sensorische Neuropathie	HMSN, axonale
es	Neuropatía axonal sensitivo-motora hereditaria	HMSN axonal
it	Malattia assonale di Charcot-Marie-Tooth
nl	Axonale erfelijke motorische en sensorische neuropathie	Axonale HMSN
pt	Neuropatia sensitiva e motora axonal hereditária	Doença de Charcot-Marie-Tooth axonal
pl	Aksonalna dziedziczna neuropatia ruchowa i czuciowa	Aksonalna HMSN
cs	Axonální hereditární senzomotorická neuropatie	Axonal HMSN · Axonální HMSN
uk	Аксональна спадкова моторна та сенсорна нейропатія	Аксональна HMSN
zh	遗传性轴突相关运动和感觉神经病	轴索HMSN
tr	Aksonal kalıtsal motor ve duyusal nöropati	Aksonal HMSN

Cross-references

qualifier = Orphanet mapping relation

Source	Code	Qualifier	ICD relation	Validation
MONDO	18775	E		validated
UMLS	C5680107	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:166Charcot-Marie-Tooth disease/Hereditary motor and sensory neuropathy
rare genetic diseases; rare neurological diseases

Children (2):

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/476109
This record as JSON: /data/d/476109.json