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Congenital thrombotic thrombocytopenic purpura due to ADAMTS-13 deficiency
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Severe hemophilia A
1 associated gene
No signs/symptoms info
Congenital thrombotic thrombocytopenic purpura due to ADAMTS-13 deficiency
Severe hemophilia A

ADAMTS13
(UniProt - OMIM)
 F8
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
ADAMTS13
(0.72)
F8


Citations in the biomedical literature:


Congenital thrombotic thrombocytopenic purpura due to ADAMTS-13 deficiency
ADAMTS13
Severe hemophilia A
F8



Congenital thrombotic thrombocytopenic purpura due to ADAMTS-13 deficiency
Severe hemophilia A

Synonym(s):
- Upshaw-Schulman syndrome
Synonym(s):
- Severe factor VIII deficiency
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
- Rare renal disease
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
Classification (ICD10):
- Diseases of the musculoskeletal system and connective tissue -
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: 1-9 / 100 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: x-linked recessive
External references:
1 OMIM reference -
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.