ODCs

Click node...

1 OMIM reference -
1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

6 associated genes
No signs/symptoms info

Familial amyloidosis, Finnish type

Familial renal cell carcinoma


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	GSN	(0.52)	FHIT

Citations in the biomedical literature:

Familial amyloidosis, Finnish type		Familial renal cell carcinoma
	Synonym(s): - Familial amyloid polyneuropathy type 4 - Gelsolin amyloidosis - Hereditary amyloidosis, Finnish type		Synonym(s): (no synonyms)

	Classification (Orphanet): - Rare eye disease - Rare genetic disease - Rare neurologic disease - Rare systemic or rheumatologic disease		Classification (Orphanet): (no data available)

	Classification (ICD10): - Endocrine, nutritional and metabolic diseases -		Classification (ICD10): - Neoplasms -

	Epidemiological data: Class of prevalence: unknown Average age onset: adulthood Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: (no data available)

	External references: 1 OMIM reference - No MeSH references		External references: No OMIM references 1 MeSH reference: C536851

No signs/symptoms info available.