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Bleeding diathesis due to thromboxane synthesis deficiency
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Familial hypocalciuric hypercalcemia type 2
1 OMIM reference -
1 associated gene
No signs/symptoms info
Bleeding diathesis due to thromboxane synthesis deficiency
Familial hypocalciuric hypercalcemia type 2

TBXA2R
(UniProt - OMIM)
 GNA11
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
TBXA2R
(0.76)
GNA11


Citations in the biomedical literature:


Bleeding diathesis due to thromboxane synthesis deficiency
TBXA2R
Familial hypocalciuric hypercalcemia type 2
GNA11



Bleeding diathesis due to thromboxane synthesis deficiency
Familial hypocalciuric hypercalcemia type 2

Synonym(s):
(no synonyms)

Synonym(s):
- FHH type 2
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
Classification (Orphanet):
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare endocrine disease
- Rare genetic disease
- Rare respiratory disease
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
(no data available)
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
External references:
1 OMIM reference -
1 MeSH reference: C537146
No signs/symptoms info available.