ODCs

Click node...

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

PROTEIN INTERACTIONS: 1

1 associated gene
No signs/symptoms info

Essential fructosuria

Familial renal amyloidosis due to lysozyme variant


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	KHK	(0.76)	LYZ

Citations in the biomedical literature:

Essential fructosuria		Familial renal amyloidosis due to lysozyme variant
	Synonym(s): - Fructokinase deficiency - Ketohexokinase deficiency		Synonym(s): - Familial amyloid nephropathy due to lysozyme variant - Hereditary amyloid nephropathy due to lysozyme variant - Hereditary renal amyloidosis due to lysozyme variant - Lysozyme amyloidosis

	Classification (Orphanet): - Inborn errors of metabolism - 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: unknown Average age onset: variable Average age of death: normal Type of inheritance: autosomal recessive		Epidemiological data: (no data available)

	External references: 1 OMIM reference - 1 MeSH reference: C538068		External references: No OMIM references No MeSH references

No signs/symptoms info available.