ODCs

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

COMMON GENES: 1

1 OMIM reference -
2 associated genes
No signs/symptoms info

Laing distal myopathy

Classic multiminicore myopathy

MYH7	(UniProt - OMIM)		MYH7	(UniProt - OMIM)
			SEPN1	(UniProt - OMIM)

Citations in the biomedical literature:

Laing distal myopathy		Classic multiminicore myopathy
	Synonym(s): - Distal myopathy type 1 - Laing early-onset distal myopathy - MPD1		Synonym(s): - Classic MmD - Classic multiminicore disease

	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: childhood Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: (no data available)

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

No signs/symptoms info available.