OMOP Concept 433257
Mesangiocapillary glomerulonephritis
StandardConditionSNOMED80321008Disorder
Maps from
22
Descendants
18
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
22 source codes normalize to Mesangiocapillary glomerulonephritis via the OMOP "Maps to" relationship.
Synonyms
Alternative names recorded for Mesangiocapillary glomerulonephritis across source vocabularies.
- glomerulonefritis crónica, forma mesangial
- glomerulonefritis membranoproliferativa
- glomerulonefritis mesangiocapilar
- glomerulonefritis mesangiocapilar (trastorno)
- Lobular glomerulonephritis
- MCGN - Mesangiocapillary glomerulonephritis
- Membranoproliferative glomerulonephritis
- Mesangiocapillary glomerulonephritis (disorder)
- MPGN - Membranoproliferative glomerulonephritis
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(36)Roll up to these when you need a wider cohort.
- 1Chronic mesangial proliferative glomerulonephritis
- 2Chronic proliferative glomerulonephritis
- 2Mesangial proliferative glomerulonephritis
- 3Chronic glomerulonephritis
- 3Glomerulonephritis
- 3Proliferative glomerulonephritis
- 4Chronic disease of genitourinary system
- 4Chronic inflammatory disorder
- 4Glomerular disease
- 4Nephritis
- 5Chronic disease
- 5Disorder of renal parenchyma
- 5Disorder of the genitourinary system
- 5Inflammation of specific body organs
- 5Inflammatory disorder
- 5Inflammatory disorder of genitourinary system
- 6Disease
- 6Disorder of abdominopelvic segment of trunk
- 6Disorder of body system
- 6Inflammation of specific body structures or tissue
- 6Inflammation of specific body systems
- 6Kidney disease
- 6Urogenital finding
- 7Clinical finding
- 7Disorder of kidney and/or ureter
Narrower concepts
(18)Included automatically when you query with descendants.
- 1C4 (complement component 4) glomerulopathy
- 1Complement component 3 glomerulopathy
- 1Focal membranoproliferative glomerulonephritis
- 1Mesangiocapillary glomerulonephritis, type I
- 1Mesangiocapillary glomerulonephritis type III
- 1Mesangiocapillary glomerulonephritis type IV
- 2Acute nephritic syndrome co-occurrent and due to membranoproliferative glomerulonephritis type III
- 2Chronic nephritic syndrome co-occurrent and due to membranoproliferative glomerulonephritis type III
- 2Complement component 3 glomerulonephritis
- 2Complement component 4 dense deposit disease
- 2Complement component 4 glomerulonephritis
- 2Dense deposit disease
- 2Hereditary nephropathy co-occurrent with membranoproliferative glomerulonephritis type III
- 2Nephritic syndrome co-occurrent and due to membranoproliferative glomerulonephritis type III
- 2Nephrotic syndrome co-occurrent and due to membranoproliferative glomerulonephritis type III
- 3Persistent hematuria co-occurrent and due to dense deposit disease
- 3Rapidly progressive nephritic syndrome co-occurrent and due to membranoproliferative glomerulonephritis type III
- 3Recurrent hematuria co-occurrent and due to dense deposit disease
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