ODCs

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1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

2 OMIM references -
1 associated gene
No signs/symptoms info

Autosomal codominant severe lipodystrophic laminopathy

Reducing body myopathy


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	LMNA	(0.49)	FHL1

Citations in the biomedical literature:

Autosomal codominant severe lipodystrophic laminopathy		Reducing body myopathy

	Classification (Orphanet): - Rare endocrine disease - Rare genetic disease - Rare skin 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: Class of prevalence: <1 / 1 000 000 Average age onset: adulthood Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: (no data available)

	External references: No OMIM references No MeSH references		External references: 2 OMIM references - No MeSH references

No signs/symptoms info available.