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Benign paroxysmal torticollis of infancy
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Von Willebrand disease type 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Benign paroxysmal torticollis of infancy
Von Willebrand disease type 1

CACNA1A
(UniProt - OMIM)
 VWF
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
CACNA1A
(0.63)
VWF


Citations in the biomedical literature:


Benign paroxysmal torticollis of infancy
CACNA1A
Von Willebrand disease type 1
VWF



Benign paroxysmal torticollis of infancy
Von Willebrand disease type 1

Synonym(s):
(no synonyms)

Synonym(s):
- Willebrand disease type 1
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: normal
Type of inheritance: sporadic
Epidemiological data:
Class of prevalence: 1-5 / 10 000
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal dominant
External references:
No OMIM references
No MeSH references
External references:
1 OMIM reference -
1 MeSH reference: D056725
No signs/symptoms info available.