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Bleeding diathesis due to thromboxane synthesis deficiency
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Generalized epilepsy - paroxysmal dyskinesia
1 OMIM reference -
1 associated gene
No signs/symptoms info
Bleeding diathesis due to thromboxane synthesis deficiency
Generalized epilepsy - paroxysmal dyskinesia

TBXA2R
(UniProt - OMIM)
 KCNMA1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
TBXA2R
(0.83)
KCNMA1


Citations in the biomedical literature:


Bleeding diathesis due to thromboxane synthesis deficiency
TBXA2R
Generalized epilepsy - paroxysmal dyskinesia
KCNMA1



Bleeding diathesis due to thromboxane synthesis deficiency
Generalized epilepsy - paroxysmal dyskinesia

Synonym(s):
(no synonyms)

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