ODCs

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1 OMIM reference -
2 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 2

1 associated gene
No signs/symptoms info

Glanzmann thrombasthenia

Familial renal amyloidosis due to fibrinogen A alpha-chain variant

ITGA2B	(UniProt - OMIM)		FGA	(UniProt - OMIM)
ITGB3	(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:

Glanzmann thrombasthenia		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: unknown Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal recessive		Epidemiological data: (no data available)

	External references: 1 OMIM reference - No MeSH references		External references: No OMIM references No MeSH references

No signs/symptoms info available.