| Descriptor English: | Glomerulonephritis, Membranoproliferative | ||||||
| Descriptor Spanish: |
Glomerulonefritis Membranoproliferativa
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| Descriptor Portuguese: | Glomerulonefrite Membranoproliferativa | ||||||
| Descriptor French: | Glomérulonéphrite membranoproliférative | ||||||
| Entry term(s): |
C3G Complement 3 Glomerulopathy Complement 3 Glomerulopathies Complement 3 Glomerulopathy DDD MPGNII Dense Deposit Disease Glomerulonephritides, Hypocomplementemic Glomerulonephritides, Membranoproliferative Glomerulonephritides, Mesangiocapillary Glomerulonephritis, Hypocomplementemic Glomerulonephritis, Mesangiocapillary Glomerulopathies, Complement 3 Glomerulopathy, Complement 3 Hypocomplementemic Glomerulonephritides Hypocomplementemic Glomerulonephritis MPGN Membranoproliferative Glomerulonephritis MPGNII Membranoproliferative Glomerulonephritides Membranoproliferative Glomerulonephritis Membranoproliferative Glomerulonephritis Type II Membranoproliferative Glomerulonephritis, Subendothelial Membranoproliferative Glomerulonephritis, Type I Membranoproliferative Glomerulonephritis, Type II Membranoproliferative Glomerulonephritis, Type III Mesangiocapillary Glomerulonephritides Mesangiocapillary Glomerulonephritis Mesangiocapillary Glomerulonephritis, Type I Mesangiocapillary Glomerulonephritis, Type II Subendothelial Membranoproliferative Glomerulonephritis Type II MPGN |
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| Tree number(s): |
C12.050.351.968.419.570.363.615 C12.200.777.419.570.363.615 C12.950.419.570.363.615 C20.425 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D015432 | ||||||
| Scope note: | Chronic glomerulonephritis characterized histologically by proliferation of MESANGIAL CELLS, increase in the MESANGIAL EXTRACELLULAR MATRIX, and a thickening of the glomerular capillary walls. This may appear as a primary disorder or secondary to other diseases including infections and autoimmune disease SYSTEMIC LUPUS ERYTHEMATOSUS. Various subtypes are classified by their abnormal ultrastructures and immune deposits. Hypocomplementemia is a characteristic feature of all types of MPGN. |
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| Annotation: | do not confuse with GLOMERULONEPHRITIS, MEMBRANOUS; do not make diagnoses: use the term used by the author |
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| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CN congenital CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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| Previous Indexing: |
Glomerulonephritis (1969-1988) |
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| Public MeSH Note: | 89 |
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| History Note: | 89 |
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| DeCS ID: | 23655 | ||||||
| Unique ID: | D015432 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 1989/01/01 | ||||||
| Date of Entry: | 1988/06/08 | ||||||
| Revision Date: | 2022/07/08 |
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Glomerulonephritis, Membranoproliferative
- Preferred
Membranoproliferative Glomerulonephritis, Type III
- Narrower
Membranoproliferative Glomerulonephritis, Type I
- Narrower
Membranoproliferative Glomerulonephritis, Type II
- Narrower
Complement 3 Glomerulopathies
- Related but not broader or narrower
| Concept UI |
M0023780 |
| Scope note | Chronic glomerulonephritis characterized histologically by proliferation of MESANGIAL CELLS, increase in the MESANGIAL EXTRACELLULAR MATRIX, and a thickening of the glomerular capillary walls. This may appear as a primary disorder or secondary to other diseases including infections and autoimmune disease SYSTEMIC LUPUS ERYTHEMATOSUS. Various subtypes are classified by their abnormal ultrastructures and immune deposits. Hypocomplementemia is a characteristic feature of all types of MPGN. |
| Preferred term | Glomerulonephritis, Membranoproliferative |
| Entry term(s) |
Glomerulonephritides, Hypocomplementemic Glomerulonephritides, Membranoproliferative Glomerulonephritides, Mesangiocapillary Glomerulonephritis, Hypocomplementemic Glomerulonephritis, Mesangiocapillary Hypocomplementemic Glomerulonephritides Hypocomplementemic Glomerulonephritis MPGN Membranoproliferative Glomerulonephritis Membranoproliferative Glomerulonephritides Membranoproliferative Glomerulonephritis Mesangiocapillary Glomerulonephritides Mesangiocapillary Glomerulonephritis |
| Concept UI |
M0490967 |
| Scope note | A type of mesangiocapillary glomerulonephritis that is characterized by subepithelial immune deposit and may be a variant of type I. |
| Preferred term | Membranoproliferative Glomerulonephritis, Type III |
| Concept UI |
M0490965 |
| Scope note | A type of mesangiocapillary glomerulonephritis that is characterized by immune deposits on the endothelial side of the GLOMERULAR BASEMENT MEMBRANE leading to splitting and reduplication of the basement membrane. |
| Preferred term | Membranoproliferative Glomerulonephritis, Type I |
| Entry term(s) |
Membranoproliferative Glomerulonephritis, Subendothelial Mesangiocapillary Glomerulonephritis, Type I Subendothelial Membranoproliferative Glomerulonephritis |
| Concept UI |
M0490966 |
| Scope note | A type of mesangiocapillary glomerulonephritis that is characterized by the dark bands of electron-dense deposits in the GLOMERULAR BASEMENT MEMBRANE caused by autoantibodies against ALTERNATIVE PATHWAY C3 CONVERTASE (C3bBb). |
| Preferred term | Membranoproliferative Glomerulonephritis, Type II |
| Entry term(s) |
DDD MPGNII Dense Deposit Disease MPGNII Membranoproliferative Glomerulonephritis Type II Mesangiocapillary Glomerulonephritis, Type II Type II MPGN |
| Concept UI |
M000756166 |
| Preferred term | Complement 3 Glomerulopathies |
| Entry term(s) |
C3G Complement 3 Glomerulopathy Complement 3 Glomerulopathy Glomerulopathies, Complement 3 Glomerulopathy, Complement 3 |
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