Details of Disease | DrugMAP

General Information of Disease (ID: DIS74WB1)

Disease Name	AApoAI amyloidosis
Synonyms	familial amyloid nephropathy due to apolipoprotein A-I variant; familial renal amyloidosis due to apolipoprotein A-I variant; hereditary renal amyloidosis due to apolipoprotein A-I variant; apolipoprotein A-I amyloidosis; hereditary amyloid nephropathy due to apolipoprotein A-I variant
Disease Hierarchy	DIS7BVSW: Familial visceral amyloidosis DIS74WB1: AApoAI amyloidosis
Disease Identifiers	MONDO ID MONDO_0019731 UMLS CUI C5680269 MedGen ID 1842920 Orphanet ID 93560

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
APOA1	TT7GN3U	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
APOA1	OT5THARI	Supportive	Autosomal dominant	[1]
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References

1	Hereditary apolipoprotein AI-associated amyloidosis in surgical pathology specimens: identification of three novel mutations in the APOA1 gene. J Mol Diagn. 2009 May;11(3):257-62. doi: 10.2353/jmoldx.2009.080161. Epub 2009 Mar 26.