ODCs

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1 OMIM reference -
4 associated genes
No signs/symptoms info

COMMON GENES: 1

2 OMIM references -
2 associated genes
No signs/symptoms info

Hyperlipoproteinemia type 5

Hyperlipoproteinemia type 4

Citations in the biomedical literature:

Hyperlipoproteinemia type 5		Hyperlipoproteinemia type 4
	Synonym(s): - Major hyperlipidemia		Synonym(s): - Familial hypertriglyceridemia

	Classification (Orphanet): - Inborn errors of metabolism - Rare endocrine disease - Rare genetic disease		Classification (Orphanet): - Inborn errors of metabolism - Rare endocrine disease - Rare genetic disease

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

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: - Average age onset: adulthood Average age of death: no data available Type of inheritance: autosomal dominant

	External references: 1 OMIM reference - 1 MeSH reference: D006954		External references: 2 OMIM references - 1 MeSH reference: D006953

No signs/symptoms info available.