ODCs

Click node...

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

COMMON GENES: 1
PROTEIN INTERACTIONS: 2

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

Hyperlipoproteinemia type 1

Hyperlipoproteinemia type 5


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	GPIHBP1 LMF1	(0.63) (0.63)	LPL LPL

Citations in the biomedical literature:

Hyperlipoproteinemia type 1		Hyperlipoproteinemia type 5
	Synonym(s): - Familial hyperchylomicronemia		Synonym(s): - Major hyperlipidemia

	Classification (Orphanet): - Rare endocrine 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: Class of prevalence: 1-9 / 1 000 000 Average age onset: childhood Average age of death: normal Type of inheritance: autosomal recessive		Epidemiological data: (no data available)

	External references: 3 OMIM references - 1 MeSH reference: D008072		External references: 1 OMIM reference - 1 MeSH reference: D006954

No signs/symptoms info available.