ODCs

Click node...

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

PROTEIN INTERACTIONS: 2

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

Lipoprotein glomerulopathy

Homozygous familial hypercholesterolemia


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	APOE APOE	(0.88) (0.49)	LDLR APOB

Citations in the biomedical literature:

Lipoprotein glomerulopathy		Homozygous familial hypercholesterolemia
	Synonym(s): - LPG		Synonym(s): - HoFH

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

	Classification (ICD10): (no data available)		Classification (ICD10): - Endocrine, nutritional and metabolic diseases -

	Epidemiological data: Class of prevalence: unknown Average age onset: variable Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: - Average age onset: - Average age of death: - Type of inheritance: autosomal recessive

	External references: 1 OMIM reference - No MeSH references		External references: 3 OMIM references - No MeSH references

No signs/symptoms info available.