Comparative

Human disease

ataxia telangiectasia

MONDO:0008840

Mondo defines it as: “Ataxia-telangiectasia is the association of severe combined immunodeficiency (affecting mainly the humoral immune response) with progressive cerebellar ataxia. It is characterized by neurological signs, telangiectasias, increased susceptibility to infections and a higher risk of cancer.”

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
2044 Ataxia telangiectasia, ATM-related Both routes 2 Target evidence 65.6

Human genes

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

Human gene Score Evidence
ATM 0.88 16,042

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
Dexamethasone Phosphoric Acid None of these genes Approved
Levacetylleucine None of these genes Phase 3
Trenonacog Alfa None of these genes Phase 3
Niacinamide None of these genes Phase 2
Baclofen None of these genes Early phase 1
Nicotinamide Riboside 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.