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Autosomal dominant macrothrombocytopenia
3 OMIM references -
4 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 2
Familial renal amyloidosis due to fibrinogen A alpha-chain variant
1 associated gene
No signs/symptoms info
Autosomal dominant macrothrombocytopenia
Familial renal amyloidosis due to fibrinogen A alpha-chain variant

ACTN1
(UniProt - OMIM)
 FGA
(UniProt - OMIM)
ITGA2B
(UniProt - OMIM)
ITGB3
(UniProt - OMIM)
TUBB1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
ITGA2B
ITGB3
(0.52)
(0.52)
FGA
FGA


Citations in the biomedical literature:


Autosomal dominant macrothrombocytopenia
ACTN1 ITGA2B ITGB3 TUBB1
Familial renal amyloidosis due to fibrinogen A alpha-chain variant
FGA



Autosomal dominant macrothrombocytopenia
Familial renal amyloidosis due to fibrinogen A alpha-chain variant

Synonym(s):
(no synonyms)

Synonym(s):
- Familial amyloid nephropathy due to fibrinogen A alpha-chain variant
- Fibrinogen A alpha-chain amyloidosis
- Hereditary amyloid nephropathy due to fibrinogen A alpha-chain variant
- Hereditary renal amyloidosis due to fibrinogen A alpha-chain variant
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare renal 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:
Class of prevalence: <1 / 1 000 000
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)
External references:
3 OMIM references -
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.