Motor Peripheral Neuropathy (HSMN)

Alias:
Peripheral Motor Neuropathy
Hsmn - Hereditary Sensory and Motor Neuropathy
Hereditary Motor and Sensory Neuropathies
Hereditary Motor and Sensory Neuropathy
Hereditary Sensory and Motor Neuropathy
Neuropathic Muscular Atrophy
Hsmn
Favorite
Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Motor Peripheral Neuropathy, also known as peripheral motor neuropathy, is related to charcot-marie-tooth disease, axonal, type 2a1 and charcot-marie-tooth disease, axonal, type 2t, and has symptoms including neurologic symptoms An important gene associated with Motor Peripheral Neuropathy is RNMT (RNA Guanine-7 Methyltransferase), and among its related pathways/superpathways are Intracellular trafficking proteins involved in CMT neuropathy and EGR2 and SOX10-mediated initiation of Schwann cell myelination. The drugs Folic acid and Lipoic acid have been mentioned in the context of this disorder. Affiliated tissues include spinal cord and breast, and related phenotypes are nervous system and homeostasis/metabolism
Related ID:
MESH:D015417

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
--
Unknown
--
28
222
--

Medical Symptom

#
Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

#
Gene
Function
Score
Mutations
No data available

Related Drugs

Name
CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

Title
PMID
Journal
Year
IF
No Data Found!
Wechat
Comparison
Al agent
Tutorials
Back to top