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Familial renal amyloidosis due to lysozyme variant
1 associated gene
10 connected diseases
No signs/symptoms info
Disease Type of connection
Essential fructosuria
Cabezas syndrome
Chuvash erythrocytosis
Mosaic variegated aneuploidy syndrome
Proximal myotonic myopathy
Von Hippel-Lindau disease
Estrogen resistance syndrome
Autosomal dominant cutis laxa
Supravalvular aortic stenosis
Williams syndrome
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):
- Rare genetic disease
- Rare renal disease
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
(no data available)
External references:
No OMIM references
No MeSH references
Gene symbol UniProt reference OMIM reference
LYZ P61626153450
No signs/symptoms info available.