ODCs

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

PROTEIN INTERACTIONS: 1

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

Hereditary motor and sensory neuropathy, Okinawa type

Myotilin-related myofibrillar myopathy without spheroid body


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	TFG	(0.63)	MYOT

Citations in the biomedical literature:

Hereditary motor and sensory neuropathy, Okinawa type		Myotilin-related myofibrillar myopathy without spheroid body
	Synonym(s): - HMSNP - Hereditary motor and sensory neuropathy, proximal type		Synonym(s): (no synonyms)

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare genetic disease - Rare neurologic disease

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): - Diseases of the nervous system -

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

	External references: 1 OMIM reference - 1 MeSH reference: C535717		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.