Details of Disease

General Information of Disease (ID: DISF51DA)

Disease Name IgA nephropathy, susceptibility to, 3
Synonyms
susceptibility to IgA nephropathy 3; IgA nephropathy, susceptibility to, type 3; SPRY2 IgA glomerulonephritis; IgA nephropathy, susceptibility to, 3; IGAN3; IGAN3; IgA nephropathy, susceptibility to, 3; IgA glomerulonephritis caused by mutation in SPRY2
Definition Any IgA glomerulonephritis in which the cause of the disease is a mutation in the SPRY2 gene.
Disease Hierarchy
DIS98MYE: Inherited disease susceptibility
DISRP5FG: IgA nephropathy, susceptibility to
DISF51DA: IgA nephropathy, susceptibility to, 3
Disease Identifiers
MONDO ID
MONDO_0014786
UMLS CUI
C4225194
OMIM ID
616818
MedGen ID
897340

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)
This Disease Is Related to 1 DOT Molecule(s)
Gene Name DOT ID Evidence Level Mode of Inheritance REF
SPRY2 OTH0CRCZ Limited Autosomal dominant [1]
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References

1 Classification of Genes: Standardized Clinical Validity Assessment of Gene-Disease Associations Aids Diagnostic Exome Analysis and Reclassifications. Hum Mutat. 2017 May;38(5):600-608. doi: 10.1002/humu.23183. Epub 2017 Feb 13.