Comparative

Human disease

cutaneous mastocytosis

MONDO:0019023

Mondo defines it as: “Cutaneous mastocytosis is a term referring to a group of diseases characterized by abnormal accumulation and proliferation of skin mastocytes. In some cases (most commonly in adults), cutaneous mastocytosis may occur in association with mast cell infiltration of various extracutaneous organs, in which case the disorder is referred to as systemic mastocytosis.”

2 disease groups in OMIA reach 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
1289 Urticaria pigmentosa OMIA's OMIM numbers 1 Human disease 29.0
2816 Mastocytosis, cutaneous OMIA's OMIM numbers 1 Human disease 29.0

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
Masitinib None of these genes Phase 3
Hydroxychloroquine None of these genes Phase 2/3
Cromolyn None of these genes Phase 2
Diphenhydramine None of these genes Phase 2
Trolamine Salicylate None of these genes Phase 2
Elenestinib None of these genes Unknown
Lirentelimab 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.