Nephrotic syndrome

Symptom Information:

Symptom ID: HPO:0000100
Synonyms:
Nephrosis [HPO:0000100]
Nephrotic syndrome (disorder) [Orphanet:38360]
Nephrotic syndrome with unspecified pathological lesion in kidney [Orphanet:38360]
Nephrotic Syndrome [Orphanet:38360]
Nephrosis [OMIM:Nephrosis]
Nephrotic syndrome [OMIM:Nephrotic syndrome]
Nephrotic syndrome [Orphanet:38360]
Nephrotic syndrome [MedDRA:10029164]
Nephrosis [MedDRA:10029164]
Nephrosis osmotic [MedDRA:10029164]
Nephrotic syndrome in diseases classified elsewhere [MedDRA:10029164]
Nephrotic syndrome with lesion of membranoproliferative glomerulonephritis [MedDRA:10029164]
Nephrotic syndrome with lesion of membranous glomerulonephritis [MedDRA:10029164]
Nephrotic syndrome with lesion of minimal change glomerulonephritis [MedDRA:10029164]
Nephrotic syndrome with lesion of proliferative glomerulonephritis [MedDRA:10029164]
Nephrotic syndrome with other pathological lesion in kidney [MedDRA:10029164]
Nephrotic syndrome with other specified pathological lesion in kidney [MedDRA:10029164]
Nephrotic syndrome with unspecified pathological lesion in kidney [MedDRA:10029164]
Syndrome nephrotic [MedDRA:10029164]
Nephrotic syndrome worsened [MedDRA:10029164]
Steroid-resistant nephrotic syndrome [MedDRA:10029164]
Nephrotic syndrome, steroid-resistant [OMIM:Nephrotic syndrome, steroid-resistant]
Quality:
Cross references:
Orphanet:38360 "Nephrotic syndrome" [Orphanet:38360]
OMIM: "Nephrosis" [OMIM:Nephrosis]
OMIM: "Nephrotic syndrome" [OMIM:Nephrotic syndrome]
OMIM: "Nephrotic syndrome, steroid-resistant" [OMIM:Nephrotic syndrome, steroid-resistant]
UMLS:C0027730 "Nephrotic syndrome with unspecified pathological lesion in kidney" [Orphanet:38360]
UMLS:C0027726 "Nephrotic Syndrome" [Orphanet:38360]
Is a (Direct Parents):
HPO         Abnormal renal physiology
Orphanet Abnormality of the urinary system physiology
MedDRA Glomerulonephritis and nephrotic syndrome
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the genitourinary system(HPO:0000119)
          Abnormality of the urinary system(HPO:0000079)
             Abnormality of the upper urinary tract(HPO:0010935)
                Abnormality of the kidney(HPO:0000077)
                   Abnormal renal physiology(HPO:0012211)
                      Nephrotic syndrome(HPO:0000100)
             Abnormality of the urinary system physiology(HPO:0011277)
                Abnormal renal physiology(HPO:0012211)
                   Nephrotic syndrome(HPO:0000100)
MedDRA:
Renal and urinary disorders(MedDRA:10038359)
    Nephropathy(HPO:0000112)
       Glomerulonephritis and nephrotic syndrome(MedDRA:10018365)
          Nephrotic syndrome(HPO:0000100)
Database Frequency: 83 / 7739
Resource:

All diseases associated with this symptom:

AA amyloidosis (Orphanet:85445)
AICARDI-GOUTIERES SYNDROME 7 (OMIM:615846)
AL amyloidosis (Orphanet:85443)
AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE IIA (OMIM:603909)
AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE III (OMIM:615559)
Action myoclonus - renal failure syndrome (Orphanet:163696)
Alagille syndrome (Orphanet:52)
Alpha-1-antitrypsin deficiency (Orphanet:60)
Alport syndrome (Orphanet:63)
Atherosclerosis - deafness - diabetes - epilepsy - nephropathy (Orphanet:1192)
Atypical hemolytic uremic syndrome with DGKE deficiency (Orphanet:357008)
Autosomal dominant beta2-microglobulinic amyloidosis (Orphanet:314652)
Autosomal recessive Alport syndrome (Orphanet:88919)
Bardet-Biedl syndrome (Orphanet:110)
CEDNIK syndrome (Orphanet:66631)
CHONDROITIN-6-SULFATURIA, DEFECTIVE CELLULAR IMMUNITY, NEPHROTIC SYNDROME (OMIM:215250)
COENZYME Q10 DEFICIENCY, PRIMARY, 1 (OMIM:607426)
COENZYME Q10 DEFICIENCY, PRIMARY, 3 (OMIM:614652)
Cockayne syndrome (Orphanet:191)
Complement component 3 deficiency (Orphanet:280133)
Congenital nephrotic syndrome, Finnish type (Orphanet:839)
Congenital nephrotic syndrome-interstitial lung disease-epidermolysis bullosa syndrome (Orphanet:306504)
Cystic fibrosis - gastritis - megaloblastic anemia (Orphanet:2575)
Denys-Drash syndrome (Orphanet:220)
Drug rash with eosinophilia and systemic symptoms (Orphanet:139402)
Dystrophic epidermolysis bullosa (Orphanet:303)
Ehlers-Danlos syndrome, musculocontractural type (Orphanet:2953)
FAMILIAL MEDITERRANEAN FEVER (OMIM:249100)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS 2 (OMIM:603965)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS 5 (OMIM:613237)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS 6 (OMIM:614131)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS 7 (OMIM:616002)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS 8 (OMIM:616032)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS 9 (OMIM:616220)
Fabry disease (Orphanet:324)
Familial LCAT deficiency (Orphanet:79293)
Familial Mediterranean fever (Orphanet:342)
Familial amyloidosis, Finnish type (Orphanet:85448)
Familial idiopathic steroid-resistant nephrotic syndrome (Orphanet:656)
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation (Orphanet:93214)
Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes (Orphanet:93216)
Familial renal amyloidosis (Orphanet:85450)
Familial steroid-resistant nephrotic syndrome with sensorineural deafness (Orphanet:280406)
Fibronectin glomerulopathy (Orphanet:84090)
Frasier syndrome (Orphanet:347)
Free sialic acid storage disease (Orphanet:834)
Free sialic acid storage disease, infantile form (Orphanet:309324)
GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 1 (OMIM:137950)
GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 2 (OMIM:601894)
Galloway-Mowat syndrome (Orphanet:2065)
HUTTERITE CEREBROOSTEONEPHRODYSPLASIA SYNDROME (OMIM:236450)
Hypoparathyroidism - deafness - renal disease (Orphanet:2237)
Idiopathic steroid-sensitive nephrotic syndrome (Orphanet:69061)
Immunoglobulin-mediated membranoproliferative glomerulonephritis (Orphanet:329903)
Insulin-resistance syndrome type A (Orphanet:2297)
LAMB-2-related infantile-onset nephrotic syndrome (Orphanet:306507)
LCAT deficiency (Orphanet:650)
LIPODYSTROPHY, PARTIAL, ACQUIRED, WITH LOW COMPLEMENT COMPONENT C3,WITH OR WITHOUT GLOMERULONEPHRITIS (OMIM:613913)
Leigh syndrome (Orphanet:506)
Leigh syndrome with nephrotic syndrome (Orphanet:255249)
MELAS (Orphanet:550)
MESANGIAL SCLEROSIS, DIFFUSE RENAL, WITH OCULAR ABNORMALITIES (OMIM:249660)
Membranous congenital glomerulonephritis due to anti-maternal neutral endopeptidase alloimmunization (Orphanet:69063)
Muckle-Wells syndrome (Orphanet:575)
Multicystic renal dysplasia (Orphanet:1851)
NEPHROSIALIDOSIS (OMIM:256150)
NEPHROTIC SYNDROME, TYPE 2 (OMIM:600995)
NEPHROTIC SYNDROME, TYPE 3 (OMIM:610725)
NEPHROTIC SYNDROME, TYPE 4 (OMIM:256370)
NEPHROTIC SYNDROME, TYPE 8 (OMIM:615244)
NEPHROTIC SYNDROME, TYPE 9 (OMIM:615573)
Nail-patella syndrome (Orphanet:2614)
Nephrosis - deafness - urinary tract - digital malformations (Orphanet:2669)
Omenn syndrome (Orphanet:39041)
PMM2-CDG (Orphanet:79318)
Partial acquired lipodystrophy (Orphanet:79087)
Pediatric systemic lupus erythematosus (Orphanet:93552)
Pierson syndrome (Orphanet:2670)
Rheumatic fever (Orphanet:3099)
Schimke immuno-osseous dysplasia (Orphanet:1830)
Sialidosis type 2 (Orphanet:87876)
Thymoma (Orphanet:99867)
X-linked Alport syndrome (Orphanet:88917)