ODCs

Click node...

1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

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

Autosomal codominant severe lipodystrophic laminopathy

Burkitt lymphoma


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	LMNA	(0.82)	MYC

Citations in the biomedical literature:

Autosomal codominant severe lipodystrophic laminopathy		Burkitt lymphoma
	Synonym(s): (no synonyms)		Synonym(s): - Small non-cleaved cell lymphoma

	Classification (Orphanet): - Rare endocrine disease - Rare genetic disease - Rare skin disease		Classification (Orphanet): - Rare hematologic disease - Rare oncologic disease

	Classification (ICD10): - Endocrine, nutritional and metabolic diseases -		Classification (ICD10): - Neoplasms -

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

	External references: No OMIM references No MeSH references		External references: 1 OMIM reference - 2 MeSH references: D002051 / D008228

No signs/symptoms info available.