raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:140450

OBSOLETE: Hereditary motor and sensory neuropathy

inactive · referred to ORPHA:166Charcot-Marie-Tooth disease/Hereditary motor and sensory neuropathy

Synonyms: OBSOLETE: HMSN

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 Charcot-Marie-Tooth disease/Hereditary motor and sensory neuropathy

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Hereditary motor and sensory neuropathyOBSOLETE: HMSN
frOBSOLETE : Neuropathie sensitivo-motrice héréditaireOBSOLETE : HMSN · OBSOLETE : NSMH
deOBSOLET: Neuropathie, motorische und sensorische, hereditäreOBSOLET: HMSN
esOBSOLETO: Neuropatía hereditaria sensitivo-motoraOBSOLETO: NHSM
itOBSOLETO: Neuropatia motoria e sensoriale ereditariaOBSOLETO: HMSN
nlOBSOLEET: Erfelijke motorische en sensorische neuropathieOBSOLEET: HMSN
ptOBSOLETO: Neuropatia sensitiva e motora hereditária
plNIEAKTUALNE: Dziedziczna neuropatia ruchowa i czuciowaNIEAKTUALNE: HMSN
csNEAKTUÁLNÍ: Hereditární motorická a senzorická neuropatie= en
ukЗАСТАРІЛО: Спадкова моторна та сенсорна нейропатіяЗАСТАРІЛО: HMSN
zh弃用:遗传性运动和感觉神经病HMSN
trEski adı: Kalıtsal motor ve duyusal nöropatiHMSN
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