Comparative

Human disease

choroideremia

MONDO:0010557

Mondo defines it as: “Choroideremia (CHM) is an X-linked chorioretinal dystrophy characterized by progressive degeneration of the choroid, retinal pigment epithelium (RPE) and retina.”

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
869 Retinal dystrophy OMIA's OMIM numbers 2 Human disease 27.0

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
Ciliary Neurotrophic Factor None of these genes Phase 2
Timrepigene Emparvovec None of these genes Phase 2
Kio-301 None of these genes Phase 1/2
Simvastatin None of these genes Phase 1/2

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