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4 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Intermediate nemaline myopathy
Familial amyloidosis, Finnish type

ACTA1 GSN
KLHL41
NEB
TPM3


INTERACTOME
ASSOCIATIONS

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



Citations in the biomedical literature:


Intermediate nemaline myopathy
ACTA1 KLHL41 NEB TPM3
Familial amyloidosis, Finnish type
GSN



Intermediate nemaline myopathy
Familial amyloidosis, Finnish type

Synonym(s):
(no synonyms)

Synonym(s):
- Familial amyloid polyneuropathy type 4
- Gelsolin amyloidosis
- Hereditary amyloidosis, Finnish type

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

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

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

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

No signs/symptoms info available.