Details of Disease | DrugMAP

General Information of Disease (ID: DIS5XAA6)

Disease Name	Apolipoprotein A-II amyloidosis
Synonyms	familial renal amyloidosis due to apolipoprotein A-II variant; hereditary amyloid nephropathy due to apolipoprotein A-II variant; AApoAII amyloidosis; familial amyloid nephropathy due to apolipoprotein A-II variant; hereditary renal amyloidosis due to apolipoprotein A-II variant
Disease Hierarchy	DIS7BVSW: Familial visceral amyloidosis DIS5XAA6: Apolipoprotein A-II amyloidosis
Disease Identifiers	MONDO ID MONDO_0016533 UMLS CUI C5679845 MedGen ID 1842484 Orphanet ID 238269

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
APOA2	TTGQA9W	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
APOA2	OTQ3HGTC	Supportive	Autosomal dominant	[1]
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References

1	A new human hereditary amyloidosis: the result of a stop-codon mutation in the apolipoprotein AII gene. Genomics. 2001 Mar 15;72(3):272-7. doi: 10.1006/geno.2000.6499.