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Von Willebrand disease type 2B
1 OMIM reference -
1 associated gene
38 connected diseases
No signs/symptoms info
Disease Type of connection
Von Willebrand disease type 1
Von Willebrand disease type 2A
Von Willebrand disease type 2M
Von Willebrand disease type 2N
Von Willebrand disease type 3
Fetal and neonatal alloimmune thrombocytopenia
Ehlers-Danlos / osteogenesis imperfecta syndrome
High bone mass osteogenesis imperfecta
Osteogenesis imperfecta type 1
Osteogenesis imperfecta type 2
Osteogenesis imperfecta type 3
Osteogenesis imperfecta type 4
Autosomal dominant macrothrombocytopenia
Glanzmann thrombasthenia
Bernard-Soulier syndrome
Congenital thrombotic thrombocytopenic purpura due to ADAMTS-13 deficiency
Von Willebrand disease, platelet type
Mild hemophilia A
Moderately severe hemophilia A
Severe hemophilia A
Symptomatic form of hemophilia A in female carriers
Caffey disease
Dermatofibrosarcoma protuberans
Ehlers-Danlos syndrome type 1
Ehlers-Danlos syndrome type 7A
Ehlers-Danlos syndrome, vascular-like type
Essential thrombocythemia
Myelofibrosis with myeloid metaplasia
Alternating hemiplegia of childhood
Amyotrophic lateral sclerosis
Benign paroxysmal torticollis of infancy
Familial or sporadic hemiplegic migraine
Familial paroxysmal ataxia
Spinocerebellar ataxia type 6
Spinocerebellar ataxia type 7
Ehlers-Danlos syndrome type 7B
Ehlers-Danlos syndrome, cardiac valvular type
Juvenile Paget disease
Synonym(s):
(no synonyms)
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: unknown
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
VWF P04275613160
No signs/symptoms info available.