Comparative

Human disease

myopathy

MONDO:0005336

Mondo defines it as: “A disease of the muscle in which the muscle fibers do not function properly. This results in muscular weakness.”

1 disease group in OMIA reaches this disease, through OMIA's own Mondo link or its OMIM numbers. The page shows the chain. It does not say whether an animal is a model of this disease.

Animal diseases

By natural-model score for this disease, highest first. The score says how complete and how well supported each chain is, by stated rules. How the score works.

OMIA group Name Found by Species The chain reached Score
693 Myopathy The group's name 5 Human disease 37.5

Human genes

Each human gene of these disease groups that Open Targets links to this disease.

Open Targets links none of these groups' human genes to this disease.

Drugs tested for this disease

Each ChEMBL drug that has been tested for this disease, and the human genes above it acts on, if any. Open Targets gives some drugs, such as most enzyme replacement therapies, no target gene.

Drug Acts on Latest stage for this disease
Aceneuramic Acid None of these genes Approved
Acetylcysteine None of these genes Phase 2/3
Cyclophosphamide Anhydrous None of these genes Phase 2/3
Dantrolene None of these genes Phase 2/3
Fludarabine None of these genes Phase 2/3
Resecabtagene Autoleucel None of these genes Phase 2/3
Sialic Acid None of these genes Phase 2
N-Acetylmannosamine None of these genes Phase 1/2
Human Immunoglobulin G None of these genes Phase 1
Simvastatin None of these genes Unknown

The drug data is ChEMBL's, under CC BY-SA 3.0, and came through Open Targets release 26.09.