DiseaseID 16287

脂性肾病

disease

NCI2016_NICHD_1602D:A syndrome characterized by proteinuria, hypoalbuminemia, and varying degrees of edema, and possibly hypercholesteremia.|NCI2016_02D:A collection of symptoms that include severe edema, proteinuria, an

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Disease: 1Symptom: 12Target: 12Links: 24
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Record Fields

Scalar fields from the final disease record.

Disease Id
16287
Core Entity Id
74337
Source Entity Count
1
Preferred Name
Lipoid Nephrosis
Name Cn
脂性肾病
Name Pinyin
Zhi Xing Shen Bing
Name En
Lipoid Nephrosis
Name Latin
Bilingual Status
complete
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Disgenet Type
disease
Mesh Class
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
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
NCI2016_NICHD_1602D:A syndrome characterized by proteinuria, hypoalbuminemia, and varying degrees of edema, and possibly hypercholesteremia.|NCI2016_02D:A collection of symptoms that include severe edema, proteinuria, and hypoalbuminemia; it is indicative of renal dysfunction.|MSH2017_2016_08_12:A condition characterized by severe PROTEINURIA, greater than 3.5 g/day in an average adult. The substantial loss of protein in the urine results in complications such as HYPOPROTEINEMIA; generalized EDEMA; HYPERTENSION; and HYPERLIPIDEMIAS. Diseases associated with nephrotic syndrome generally cause chronic kidney dysfunction.|HPO2016_07_04:Nephrotic syndrome is a collection of findings resulting from glomerular dysfunction with an increase in glomerular capillary wall permeability associated with pronounced proteinuria. Nephrotic syndrome refers to the constellation of clinical findings that result from severe renal loss of protein, with Proteinuria and hypoalbuminemia, edema, and hyperlipidemia. [HPO:probinson]|CSP2006:diseases involving defective kidney glomeruli, characterized by massive proteinuria and lipiduria with varying degrees of edema, hypoalbuminemia, and hyperlipidemia.|CHV2011_02:a kidney disease characterized by a high protein level in urine|AIR93:Nephrotic Syndrome: twenty-four hour urine protein > three grams. May be associated with hypoalbuminemia and hypercholesterolemia.
Version
v1
Suppressed
No

Names

Preferred names, aliases, and source labels retained in the final schema.

Name
Lipoid Nephrosis
Role
preferred
Name
Idiopathic Nephrotic Syndrome
Role
preferred
Name
Nephrotic Syndrome
Role
preferred
Name
Nephrotic Syndrome, Steroid-Resistant, Autosomal Recessive
Role
preferred
Name
Nephrotic Syndrome, Type 2
Role
preferred
Name
Nephrotic Syndrome, Type 3
Role
preferred
Name
Finnish Congenital Nephrotic Syndrome
Role
preferred
Name
Glomerulonephritis, Minimal Change
Role
preferred
Name
Nephrosis, Congenital
Role
preferred
Name
Nephrotic Syndrome, Minimal Change
Role
preferred
Name
Congenital Nephrosis
Role
alias
Name
Congenital Nephrotic Syndrome
Role
alias
Name
Familial Nephrotic Syndrome
Role
alias
Name
Finnish Congenital Nephrosis
Role
alias
Name
Minimal Change Disease
Role
alias
Name
Minimal Change Glomerulonephritis
Role
alias
Name
Minimal Change Nephropathy
Role
alias
Name
NEPHROTIC SYNDROME, EARLY-ONSET, TYPE 3
Role
alias
Name
NPHS2
Role
alias
Name
NPHS3
Role
alias
Name
Nephrosis
Role
alias
Name
Nephrosis, Lipoid
Role
alias
Name
Nephrotic Syndrome Type 1
Role
alias
Name
Nephrotic Syndrome Type 2
Role
alias
Name
Nephrotic Syndrome, Congenital
Role
alias
Name
Nephrotic Syndrome, Idiopathic
Role
alias
Name
Nephrotic Syndrome, Idiopathic, Steroid-Resistant
Role
alias
Name
Nephrotic Syndrome, Unspecified
Role
alias
Name
SRN1
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Hpo
HP:0000100HP:0008677HP:0012579
Herb
HBDIS002094HBDIS002095HBDIS008879HBDIS014746HBDIS014747HBDIS016907HBDIS018466HBDIS021539HBDIS021552
Me Sh
D009402
Omim
256300600995610725
Umls
C0027721C1853124C1868672C3496337
Icd10
N04.9
Sym Map
SMDE00079SMDE00878SMDE09765SMDE10462SMDE11385SMDE11387
Do Class
DOID:630DOID:7
Dis Ge Net
C0027721C0027726C0403399C1704320C1704321C1853124C1868672C3496337C3501848
Umls Sty
T047
Hpo Class
HP:0000119HP:0002715
Me Sh Class
C12C13
Tcmbank Disease
19678199072019821331216023352366379042924417
Itcmdb Generated
ITX-DISEASE-250D3F95EA94ITX-DISEASE-4312B3C9D881ITX-DISEASE-AA3B67888055

Attributes

Merged source attributes and domain-specific metadata.

Version
v1v1,v2v2
Suppress
0
Do Class Name
disease of anatomical entitygenetic disease; disease of anatomical entity
Disease Type
diseasegroup
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
Disease or Syndrome
Disease Definition
NCI2016_NICHD_1602D:A syndrome characterized by proteinuria, hypoalbuminemia, and varying degrees of edema, and possibly hypercholesteremia.|NCI2016_02D:A collection of symptoms that include severe edema, proteinuria, and hypoalbuminemia; it is indicative of renal dysfunction.|MSH2017_2016_08_12:A condition characterized by severe PROTEINURIA, greater than 3.5 g/day in an average adult. The substantial loss of protein in the urine results in complications such as HYPOPROTEINEMIA; generalized EDEMA; HYPERTENSION; and HYPERLIPIDEMIAS. Diseases associated with nephrotic syndrome generally cause chronic kidney dysfunction.|HPO2016_07_04:Nephrotic syndrome is a collection of findings resulting from glomerular dysfunction with an increase in glomerular capillary wall permeability associated with pronounced proteinuria. Nephrotic syndrome refers to the constellation of clinical findings that result from severe renal loss of protein, with Proteinuria and hypoalbuminemia, edema, and hyperlipidemia. [HPO:probinson]|CSP2006:diseases involving defective kidney glomeruli, characterized by massive proteinuria and lipiduria with varying degrees of edema, hypoalbuminemia, and hyperlipidemia.|CHV2011_02:a kidney disease characterized by a high protein level in urine|AIR93:Nephrotic Syndrome: twenty-four hour urine protein > three grams. May be associated with hypoalbuminemia and hypercholesterolemia.NCI2016_NICHD_1602D:Nephrotic syndrome for which no cause has been identified.|NCI2016_02D:Nephrotic syndrome for which no cause has been identified.(NICHD)NCI2016_NICHD_1602D:Nephrotic syndrome that demonstrates little histologic evidence of pathology by light microscopy; ultra-structural change is evident under electron microscopy, demonstrating diffuse effacement and fusion of podocyte processes.|NCI2016_02D:A glomerular disorder characterized by the electron microscopic finding of loss of podocyte foot processes. Light microscopic examination does not show glomerular changes. Patients present with proteinuria and nephrotic syndrome.|MSH2017_2016_08_12:A kidney disease with no or minimal histological glomerular changes on light microscopy and with no immune deposits. It is characterized by lipid accumulation in the epithelial cells of KIDNEY TUBULES and in the URINE. Patients usually show NEPHROTIC SYNDROME indicating the presence of PROTEINURIA with accompanying EDEMA.|HPO2016_07_04:The presence of minimal changes visible by light microscopy but flattened and fused podocyte foot processes on electron microscopy in a person with nephrotic range proteinuria. [Eurenomics:fschaefer]
Me Sh Disease Class
Male Urogenital Diseases; Female Urogenital Diseases and Pregnancy Complications
Dis Ge Net Disease Type
diseasegroup
Disease Class Name Me Sh
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Umls Semantic Type Name
Disease or Syndrome