Orphanet: Autosomal recessive intermediate Charcot Marie Tooth disease

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Autosomal recessive intermediate Charcot-Marie-Tooth disease

ORPHA:268337

Classification level: Group of disorders

Synonym(s):
- RI-CMT
Prevalence: -
Inheritance: Autosomal recessive
Age of onset: -
ICD-10: -
OMIM: -
UMLS: C5679732
MeSH: -
GARD: 12452
MedDRA: -

Summary

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.

Detailed information

General public

Article for general public
Svenska (2020) - Socialstyrelsen

Guidelines

Clinical practice guidelines
Deutsch (2015) - AWMF
Français (2020) - PNDS

Anesthesia guidelines
Czech (2014) - Orphananesthesia
Deutsch (2022) - Orphananesthesia
English (2022) - Orphananesthesia
Español (2022) - Orphananesthesia

Clinical Outcome Assessment (COA)

Patient-Centered Outcome Measures (PCOMs)
English (2023) - PROQOLID^TM

produced/endorsed by ERN(s) FSMR

produced/endorsed by FSMR(s)

Additional information

Further information on this disease

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Research activities on this disease

Specialised Social Services

Eurordis directory

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