Comparative

Human disease

nemaline myopathy 5

MONDO:0011539

Mondo defines it as: “Amish nemaline myopathy is a type of nemaline myopathy (NM) only observed in several families of the Amish community.”

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
2285 Muscular dystrophy, TNNT1-related OMIA's OMIM numbers 1 Target evidence 56.5

Human genes

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

Human gene Score Evidence
TNNT1 0.79 325

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.

No drug has been tested for this disease.