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Von Willebrand disease type 2M
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Congenital thrombotic thrombocytopenic purpura due to ADAMTS-13 deficiency
1 OMIM reference -
1 associated gene
No signs/symptoms info
Von Willebrand disease type 2M
Congenital thrombotic thrombocytopenic purpura due to ADAMTS-13 deficiency

VWF
(UniProt - OMIM)
 ADAMTS13
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
VWF
(0.89)
ADAMTS13


Citations in the biomedical literature:


Von Willebrand disease type 2M
VWF
Congenital thrombotic thrombocytopenic purpura due to ADAMTS-13 deficiency
ADAMTS13



Von Willebrand disease type 2M
Congenital thrombotic thrombocytopenic purpura due to ADAMTS-13 deficiency

Synonym(s):
(no synonyms)

Synonym(s):
- Upshaw-Schulman syndrome
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
- Rare renal disease
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Classification (ICD10):
- Diseases of the musculoskeletal system and connective tissue -
Epidemiological data:
Class of prevalence: unknown
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.