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Sickle Cell Disease Ontology
Last uploaded:
May 6, 2021
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| Id | http://purl.obolibrary.org/obo/SCDO_0000743
http://purl.obolibrary.org/obo/SCDO_0000743
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|---|---|
| Preferred Name | Membranous Nephropathy |
| Definitions |
A type of glomerulonephropathy characterized by histology with thickening of the basement membrane and deposition of immune complexes in the subepithelial space.
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| Synonyms |
Membranous Glomerulopathy
MN
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| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| definition | A type of glomerulonephropathy characterized by histology with thickening of the basement membrane and deposition of immune complexes in the subepithelial space. |
|---|---|
| skos:prefLabel | Membranous Nephropathy
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| rdfs:label | Membranous Nephropathy
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| prefLabel | Membranous Nephropathy
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| database cross reference | HP:0012578
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| has age of onset | Typically seen in adult population; rare in children.
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| is caused by | Idiopathic - may be related to M-type phosplipase A2 receptor antibodies; secondary forms may be related to autoimmune disease, underlying maligancies, drugs or infections. Has been reported in patients with sickle cell disease.
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| is characterised by | Nephrotic syndrome with histologic features specific to membranous nephropathy.
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| treated with | |
| definition source | |
| prefixIRI | SCDO:0000743
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| subClassOf | |
| curator note | Suggest update to description in HPO
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| type | |
| existence in other ontologies | Suggest update to description
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| hasExactSynonym |
Membranous Glomerulopathy
MN
|
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