ODCs

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1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

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

Laminopathy type Decaudain-Vigouroux

Autosomal dominant spastic paraplegia type 8


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	LMNA	(0.63)	KIAA0196

Citations in the biomedical literature:

Laminopathy type Decaudain-Vigouroux		Autosomal dominant spastic paraplegia type 8
	Synonym(s): - Laminopathy with severe metabolic syndrome and myopathy		Synonym(s): - SPG8

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

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

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: - Average age of death: - Type of inheritance: autosomal dominant

	External references: No OMIM references No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: C536867

No signs/symptoms info available.