Comparative

Human disease

Becker muscular dystrophy

MONDO:0010311

Mondo defines it as: “Becker muscular dystrophy (BMD) is a neuromuscular disease characterized by progressive muscle wasting and weakness due to degeneration of skeletal, smooth and cardiac muscle.”

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
1888 Muscular dystrophy, Becker type Both routes 3 Drug 93.7

Human genes

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

Human gene Score Evidence
DMD 0.82 2,434

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
Delandistrogene Moxeparvovec DMD Approved
Ataluren None of these genes Phase 3
Enalapril None of these genes Phase 3
(+)-Epicatechin None of these genes Phase 2
(-)-Epicatechin None of these genes Phase 2
Givinostat None of these genes Phase 2
L-Citrulline None of these genes Phase 2
Metformin None of these genes Phase 2
Pemirolast None of these genes Phase 2
Prednisone None of these genes Phase 2
Sevasemten None of these genes Phase 2
Vamorolone None of these genes Phase 2
Filgrastim None of these genes Phase 1
Gentamicin None of these genes Phase 1
Tadalafil None of these genes Early phase 1

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