Details of Disease

General Information of Disease (ID: DISQYQQT)

Disease Name Lipoprotein glomerulopathy
Synonyms LPG; lipoprotein glomerulopathy
Disease Hierarchy
DISPGGVL: Syndromic dyslipidemia
DISQYQQT: Lipoprotein glomerulopathy
Disease Identifiers
MONDO ID
MONDO_0012725
UMLS CUI
C2673196
OMIM ID
611771
MedGen ID
382034
Orphanet ID
329481
SNOMED CT ID
446923008

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)
This Disease Is Related to 2 DTT Molecule(s)
Gene Name DTT ID Evidence Level Mode of Inheritance REF
APOE TTKS9CB Strong Autosomal dominant [1]
FCER1G TTDGEC0 Strong Biomarker [2]
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This Disease Is Related to 1 DOT Molecule(s)
Gene Name DOT ID Evidence Level Mode of Inheritance REF
APOE OTFOWL2H Strong Autosomal dominant [1]
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References

1 The Gene Curation Coalition: A global effort to harmonize gene-disease evidence resources. Genet Med. 2022 Aug;24(8):1732-1742. doi: 10.1016/j.gim.2022.04.017. Epub 2022 May 4.
2 Macrophage impairment produced by Fc receptor gamma deficiency plays a principal role in the development of lipoprotein glomerulopathy in concert with apoE abnormalities.Nephrol Dial Transplant. 2012 Oct;27(10):3899-907. doi: 10.1093/ndt/gfs329. Epub 2012 Aug 3.