ID: 20

Disease Name: Hereditary lysozyme Amyloidosis

Description: 

Disease Type: Amyloidosis

ISA Name: ALys Amyloidosis

ICD-10 Classification: Amyloidosis

Tissue: Liver, Kidney, Gastrointestinal Tract, Spleen, Lymph Node, Skin, Lachrymal Gland, Salivary Gland, Heart

Cross References
http://apps.who.int/classifications/icd10/browse/2016/en#/E85

https://www.omim.org/entry/105200

https://www.ncbi.nlm.nih.gov/pubmed/8464497

https://www.ncbi.nlm.nih.gov/pubmed/28963698

https://www.ncbi.nlm.nih.gov/pubmed/25217048

https://www.ncbi.nlm.nih.gov/pubmed/21988333

Alternative Names:
Familial amyloid nephropathy due to lysozyme variant
Familial renal amyloidosis due to lysozyme variant
Hereditary amyloid nephropathy due to lysozyme variant
Hereditary renal amyloidosis due to lysozyme variant
Lysozyme amyloidosis
Hereditary Lysozyme Amyloidosis
Amyloidosis VIII
Ostertag Type Amyloidosis
German Type Amyloidosis
Amyloidosis, Familial renal
Amyloidosis, Familial visceral
Amyloidosis, Systemic Non-neuropathic

Precursor Proteins:
P61626 | Lysozyme C


Co-deposited Proteins:
No information available



Link to Amyloidosis: 
	No information available
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