ODCs

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

PROTEIN INTERACTIONS: 1

6 associated genes
No signs/symptoms info

Familial amyloidosis, Finnish type

Childhood-onset nemaline myopathy


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	GSN	(0.96)	ACTA1

Citations in the biomedical literature:

Familial amyloidosis, Finnish type		Childhood-onset nemaline myopathy
	Synonym(s): - Familial amyloid polyneuropathy type 4 - Gelsolin amyloidosis - Hereditary amyloidosis, Finnish type		Synonym(s): - Mild nemaline myopathy

	Classification (Orphanet): - Rare eye disease - Rare genetic disease - Rare neurologic disease - Rare systemic or rheumatologic disease		Classification (Orphanet): - Rare genetic disease - Rare neurologic disease

	Classification (ICD10): - Endocrine, nutritional and metabolic diseases -		Classification (ICD10): - Diseases of the nervous system -

	Epidemiological data: Class of prevalence: unknown Average age onset: adulthood Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: childhood Average age of death: - Type of inheritance: autosomal dominant

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

No signs/symptoms info available.