Muscular Dystrophy
Alias:
Muscular Dystrophies
Pseudohypertrophic Muscular Dystrophy
Pseudohypertrophic Muscle Paralysis
Pseudohypertrophic Muscular Atrophy
Progressive Musclular Dystrophy
Pseudohypertrophic Paralysis
Gower's Muscular Dystrophy
Pseudohypertrophic Atrophy
Pseudomuscular Hypertrophy
Dystrophy, Muscular
Basic Information
Medical Symptom
Gene & Mutation
Drugs
Disease Model
References
Muscular Dystrophy, also known as muscular dystrophies, is related to muscular dystrophy, congenital, lmna-related and limb-girdle muscular dystrophy, and has symptoms including back pain, muscle cramp and myoclonus. An important gene associated with Muscular Dystrophy is DMD (Dystrophin), and among its related pathways/superpathways are DREAM Repression and Dynorphin Expression and Acute viral myocarditis. The drugs Carvedilol and Ramipril have been mentioned in the context of this disorder. Affiliated tissues include skeletal muscle and spinal cord, and related phenotypes are muscle and homeostasis/metabolism
Related ID:
MESH:D009136
ICD11:1464662404
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Models
Reference
MALACARDS
--
Unknown
--
7
107
40
Medical Symptom
#
Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available
Gene & Mutation
#
Gene
Function
Score
Count
No data available
Drugs
Name
CAS Number
Status
Phase
No data available
Disease Model
Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available
References
Title
PMID
Journal
Year
IF
No Data Found!
Wechat
Comparison
Al agent
Back to top