ODCs

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

PROTEIN INTERACTIONS: 1

1 associated gene
No signs/symptoms info

Familial LCAT deficiency

Familial renal amyloidosis due to Apolipoprotein AII variant


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	LCAT	(0.49)	APOA2

Citations in the biomedical literature:

Familial LCAT deficiency		Familial renal amyloidosis due to Apolipoprotein AII variant
	Synonym(s): - Complete LCAT deficiency - FLD - Norum disease		Synonym(s): - Apolipoprotein AII amyloidosis - Familial amyloid nephropathy due to apolipoprotein AII variant - Hereditary amyloid nephropathy due to Apolipoprotein AII variant - Hereditary renal amyloidosis due to apolipoprotein AII variant

	Classification (Orphanet): - Inborn errors of metabolism - Rare endocrine disease - Rare eye disease - Rare genetic disease - Rare hematologic disease - Rare renal 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: <1 / 1 000 000 Average age onset: variable Average age of death: normal Type of inheritance: autosomal recessive		Epidemiological data: (no data available)

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

No signs/symptoms info available.