Intermediate nemaline myopathy |
Spinocerebellar ataxia type 5 |
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INTERACTOME ASSOCIATIONS (click on a score value to see the evidence) |
ACTA1
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Citations in the biomedical literature:
Intermediate nemaline myopathy |
Spinocerebellar ataxia type 5 |
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Synonym(s): (no synonyms)
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Synonym(s): - SCA5
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Classification (Orphanet): - Rare genetic disease - Rare neurologic disease
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Classification (Orphanet): - Rare genetic disease - Rare neurologic disease
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Classification (ICD10): - Diseases of the nervous system -
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Classification (ICD10): - Diseases of the nervous system -
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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
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Epidemiological data: Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
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External references: No OMIM references No MeSH references | |
External references: 1 OMIM reference - No MeSH references
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No signs/symptoms info available.