ODCs

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

PROTEIN INTERACTIONS: 1

1 associated gene
No signs/symptoms info

Homozygous familial hypercholesterolemia

Familial renal amyloidosis due to Apolipoprotein AI variant


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	APOB	(0.75)	APOA1

Citations in the biomedical literature:

Homozygous familial hypercholesterolemia		Familial renal amyloidosis due to Apolipoprotein AI variant
	Synonym(s): - HoFH		Synonym(s): - Apolipoprotein AI amyloidosis - Familial amyloid nephropathy due to apolipoprotein AI variant - Hereditary amyloid nephropathy due to apolipoprotein AI variant - Hereditary renal amyloidosis due to apolipoprotein AI variant

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

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

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

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

No signs/symptoms info available.