Comparative

Human disease

von Willebrand disease 1

MONDO:0008668

Mondo defines it as: “Type 1 von Willebrand disease (type 1 VWD) is a form of VWD characterized by a bleeding disorder associated with a partial quantitative plasmatic deficiency of an otherwise structurally and functionally normal Willebrand factor (von Willebrand factor; VWF).”

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
1056 Von Willebrand disease, generic OMIA's OMIM numbers 6 Drug 65.1
1057 Von Willebrand disease I OMIA's OMIM numbers 2 Drug 62.1

Human genes

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

Human gene Score Evidence
VWF 0.79 416

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.