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

Autosomal dominant limb-girdle muscular dystrophy type 1A

Spastic paraplegia-optic atrophy-neuropathy syndrome


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

Citations in the biomedical literature:

Autosomal dominant limb-girdle muscular dystrophy type 1A		Spastic paraplegia-optic atrophy-neuropathy syndrome
	Synonym(s): - LGMD1A - Limb-girdle muscular dystrophy due to myotilin deficiency		Synonym(s): - SPOAN

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare eye disease - 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: <1 / 1 000 000 Average age onset: adulthood Average age of death: normal 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.