Details of Disease | DrugMAP

General Information of Disease (ID: DIS4X1TS)

Disease Name	ALys amyloidosis
Synonyms	lysozyme amyloidosis; hereditary amyloid nephropathy due to lysozyme variant; familial renal amyloidosis due to lysozyme variant; familial amyloid nephropathy due to lysozyme variant; hereditary renal amyloidosis due to lysozyme variant
Disease Hierarchy	DIS7BVSW: Familial visceral amyloidosis DIS4X1TS: ALys amyloidosis
Disease Identifiers	MONDO ID MONDO_0019732 UMLS CUI C5680270 MedGen ID 1842307 Orphanet ID 93561

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)

This Disease Is Related to 1 DTT Molecule(s)

Gene Name	DTT ID	Evidence Level	Mode of Inheritance	REF
LYZ	TTAOZBW	Supportive	Autosomal dominant	[1]
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This Disease Is Related to 1 DOT Molecule(s)

Gene Name	DOT ID	Evidence Level	Mode of Inheritance	REF
LYZ	OTD7H0G6	Supportive	Autosomal dominant	[1]
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References

1	Hereditary renal amyloidosis caused by a new variant lysozyme W64R in a French family. Kidney Int. 2002 Mar;61(3):907-12. doi: 10.1046/j.1523-1755.2002.00205.x.