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Von Willebrand disease, platelet type
1 OMIM reference -
1 associated gene
34 connected diseases
No signs/symptoms info
Disease Type of connection
Bernard-Soulier syndrome
Fetal and neonatal alloimmune thrombocytopenia
Von Willebrand disease type 1
Von Willebrand disease type 2A
Von Willebrand disease type 2B
Von Willebrand disease type 2M
Von Willebrand disease type 2N
Von Willebrand disease type 3
Congenital factor XII deficiency
Hereditary angioedema type 3
Cerebral sinovenous thrombosis
Congenital factor II deficiency
Atelosteogenesis type I
Atelosteogenesis type III
Autosomal dominant Larsen syndrome
Boomerang dysplasia
Spondylocarpotarsal synostosis
Congenital factor XI deficiency
Chronic intestinal pseudoobstruction
Congenital short bowel syndrome
Congenital valvular dysplasia
Ehlers-Danlos syndrome with periventricular heterotopia
Frontometaphyseal dysplasia
Osteodysplasty, Melnick-Needles type
Otopalatodigital syndrome type 1
Otopalatodigital syndrome type 2
Periventricular nodular heterotopia
Terminal osseous dysplasia - pigmentary defects
17p13.3 microduplication syndrome
Distal 17p13.3 microdeletion syndrome
Miller-Dieker syndrome
Myxoid / round cell liposarcoma
22q11.2 deletion syndrome
Congenital high-molecular-weight kininogen deficiency
Synonym(s):
- PT-VWD
- Pseudo-Von Willebrand disease
- Pseudo-Von Willebrand disease type 2B
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
GP1BA P07359606672
No signs/symptoms info available.