DiseaseID 4086
肾病综合征7型
disease
MSH2017_2016_08_12:A type of mesangiocapillary glomerulonephritis that is characterized by subepithelial immune deposit and may be a variant of type I.
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Disease: 1Symptom: 4Target: 12Links: 16
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 4086
- Core Entity Id
- 60380
- Source Entity Count
- 1
- Preferred Name
- Nephrotic Syndrome, Type 7
- Name Cn
- 肾病综合征7型
- Name Pinyin
- Shen Bing Zong He Zheng 7 Xing
- Name En
- Nephrotic Syndrome, Type 7
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Anatomical Abnormality
- Disgenet Type
- disease
- Mesh Class
- Immune System Diseases; Male Urogenital Diseases; Female Urogenital Diseases and Pregnancy Complications
- Do Class
- disease of anatomical entitydisease of anatomical entity; genetic disease
- Hpo Class
- Abnormality of the genitourinary systemAbnormality of the immune system; Abnormality of the genitourinary system
- Mesh Class Name
- Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Immune System Diseases
- Hpo Class Name
- Abnormality of the genitourinary systemAbnormality of the genitourinary system; Abnormality of the immune system
- Do Class Name
- disease of anatomical entitygenetic disease; disease of anatomical entity
- Disease Definition
- MSH2017_2016_08_12:A type of mesangiocapillary glomerulonephritis that is characterized by subepithelial immune deposit and may be a variant of type I.
- Version
- v1,v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Nephrotic Syndrome, Type 7
Role
preferred
Name
Glomerulonephritis, Membranoproliferative
Role
preferred
Name
Membranoproliferative Glomerulonephritis, Type I
Role
preferred
Name
Membranoproliferative Glomerulonephritis, Type Ii
Role
preferred
Name
Membranoproliferative Glomerulonephritis, Type Iii
Role
preferred
Name
Glomerular Subendothelial Electron-Dense Deposits
Role
preferred
Name
HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 7
Role
preferred
Name
AHUS, SUSCEPTIBILITY TO, 7
Role
alias
Name
AHUS7
Role
alias
Name
Dense Deposit Disease
Role
alias
Name
Membranoproliferative Glomerulonephritis
Role
alias
Name
Membranoproliferative Glomerulonephritis Type Ii
Role
alias
Name
Mesangiocapillary Glomerulonephritis
Role
alias
Name
Mpgn
Role
alias
Name
NEPHROTIC SYNDROME, TYPE 7, WITH MEMBRANOPROLIFERATIVE GLOMERULONEPHRITIS
Role
alias
Name
NPHS7
Role
alias
Name
Nephrotic Syndrome Type 7
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Hpo
HP:0000793HP:0004746
Herb
HBDIS001178HBDIS006406HBDIS006407HBDIS014906HBDIS021842HBDIS022284HBDIS026548
Me Sh
D015432
Omim
615008
Umls
C0017662C0268742C0268743C1720821C3554330C3808620
Sym Map
SMDE01828SMDE09059SMDE10829SMDE10830SMDE10831
Do Class
DOID:630DOID:7
Dis Ge Net
C0017662C0268742C0268743C1720821C3554330C3808620C4476539
Umls Sty
T033T047T190
Hpo Class
HP:0000119HP:0002715
Me Sh Class
C12C13C20
Tcmbank Disease
1180415057217442176130528324349705
Itcmdb Generated
ITX-DISEASE-1AA77AC041A0ITX-DISEASE-1F05629ABE22ITX-DISEASE-800C4A2F63AEITX-DISEASE-A5EF3B5B3B2EITX-DISEASE-C6F730A722EE
Attributes
Merged source attributes and domain-specific metadata.
Version
v1,v2v2
Suppress
0
Do Class Name
disease of anatomical entitygenetic disease; disease of anatomical entity
Disease Type
diseasephenotype
Hpo Class Name
Abnormality of the genitourinary systemAbnormality of the genitourinary system; Abnormality of the immune system
Do Disease Class
disease of anatomical entitydisease of anatomical entity; genetic disease
Hpo Disease Class
Abnormality of the genitourinary systemAbnormality of the immune system; Abnormality of the genitourinary system
Umls Disease Type
Anatomical AbnormalityDisease or SyndromeFinding
Disease Definition
MSH2017_2016_08_12:A type of mesangiocapillary glomerulonephritis that is characterized by subepithelial immune deposit and may be a variant of type I.NCI2016_NICHD_1602D:Glomerulonephritis characterized by mesangial proliferation, endocapillary proliferation, and glomerular capillary wall remodeling with immune complex deposits from classical complement pathway activation.|NCI2016_02D:Glomerulonephritis characterized by mesangial proliferation, endocapillary proliferation, and glomerular capillary wall remodeling with immune complex deposits from classical complement pathway activation.(NICHD)|MSH2017_2016_08_12: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.NCI2016_NICHD_1602D:Proliferative glomerulonephritis characterized by activation of the alternative complement pathway, resulting in mesangial hypercellularity, endocapillary proliferation, and glomerular basement membrane intramembranous highly electron dense deposits.|NCI2016_02D:Proliferative glomerulonephritis characterized by activation of the alternative complement pathway, resulting in mesangial hypercellularity, endocapillary proliferation, and glomerular basement membrane intramembranous highly electron dense deposits.(NICHD)|MSH2017_2016_08_12: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).|HPO2016_07_04:A type of membranoproliferative glomerulonephritis characterized by electron dense deposits at the glomerular basement membrane. [Eurenomics:ewuehl, pmid:20301598]NCI2016_NICHD_1602D:Proliferative glomerulonephritis characterized by mesangial hypercellularity, endocapillary proliferation and glomerular capillary wall remodeling.|NCI2016_02D:Inflammation of the glomeruli characterized by deposits at the intraglomerular mesangium, resulting in thickening of the glomerular basement membrane, activation of complement, and impaired kidney function secondary to damaged glomeruli.|MSH2017_2016_08_12: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.|HPO2016_07_04:Proliferation of mesangial cells, increase in the mesangial extracellular matrix, and a thickening of the glomerular capillary walls. [Eurenomics:fschaefer, MeSH:D015432]
Me Sh Disease Class
Immune System Diseases; Male Urogenital Diseases; Female Urogenital Diseases and Pregnancy Complications
Dis Ge Net Disease Type
diseasephenotype
Disease Class Name Me Sh
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Immune System Diseases
Umls Semantic Type Name
Anatomical AbnormalityDisease or SyndromeFinding