Lipoprotein glomerulopathy

Preferred Label : Lipoprotein glomerulopathy;

Symbol : LPG;

CISMeF acronym : LPG;

Type : Phenotype, molecular basis known;

Description : Lipoprotein glomerulopathy is an uncommon kidney disease characterized by proteinuria, progressive kidney failure, and distinctive lipoprotein thrombi in glomerular capillaries (Saito et al., 2006). It mainly affects people of Japanese and Chinese origin; in these populations, it is associated with mutations in the gene that encodes apolipoprotein E (APOE; 107741). The disorder had rarely been described in Caucasians.;

Prefixed ID : #611771;

Details

Origin ID

611771;

UMLS CUI

C2673196;

Automatic exact mappings (from CISMeF team)
- APOE wt Allele [NCIt concept]
- Lipoprotein glomerulopathy [ICD-11 Category]
- Liquefied petroleum gas (substance) [SNOMED CT concept]
- penicillin G benzathine [MeSH Descriptor]
Currated CISMeF NLP mapping
- Lipoprotein glomerulopathy [ORDO Disease]
- Lipoprotein glomerulopathy (disorder) [SNOMED CT concept]
- lipoprotein glomerulopathy [MeSH concept]
- lipoprotein glomerulopathy [MeSH Supplementary Concept]
Genes related to phenotype
- Apolipoprotein e [OMIM gene]
HPO term(s)
- Glomerulopathy [HPO term]
- Mesangial hypercellularity [HPO term]
- Proteinuria [HPO term]
- Renal insufficiency [HPO term]
ORDO concept(s)
- Lipoprotein glomerulopathy [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Lipoprotein glomerulopathy [ORDO Disease]
- Lipoprotein glomerulopathy (disorder) [SNOMED CT concept]
- lipoprotein glomerulopathy [MeSH Supplementary Concept]
- lipoprotein glomerulopathy [MeSH concept]

Keyword's position in hierarchy(ies) :

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