ODCs

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

PROTEIN INTERACTIONS: 1

1 associated gene
No signs/symptoms info

Autosomal dominant spastic paraplegia type 8

Autosomal codominant severe lipodystrophic laminopathy


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

Citations in the biomedical literature:

Autosomal dominant spastic paraplegia type 8		Autosomal codominant severe lipodystrophic laminopathy
	Synonym(s): - SPG8		Synonym(s): (no synonyms)

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

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

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: - Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: adulthood Average age of death: - Type of inheritance: autosomal dominant

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

No signs/symptoms info available.