ODCs

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1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

2 associated genes
No signs/symptoms info

Autosomal codominant severe lipodystrophic laminopathy

Craniopharyngioma

LMNA	(UniProt - OMIM)		BRAF	(UniProt - OMIM)
			CTNNB1	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	LMNA	(0.63)	CTNNB1

Citations in the biomedical literature:

Autosomal codominant severe lipodystrophic laminopathy		Craniopharyngioma

	Classification (Orphanet): - Rare endocrine disease - Rare genetic disease - Rare skin disease		Classification (Orphanet): - Rare endocrine disease - Rare neurologic 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: 1-9 / 100 000 Average age onset: variable Average age of death: - Type of inheritance: sporadic

	External references: No OMIM references No MeSH references		External references: No OMIM references 1 MeSH reference: D003397

No signs/symptoms info available.