Nephrotic syndrome
Symptom Information:
Symptom ID: | HPO:0000100 | ||||||||||||||||||||||
Synonyms: |
|
||||||||||||||||||||||
Quality: | |||||||||||||||||||||||
Cross references: |
|
||||||||||||||||||||||
Is a (Direct Parents): |
|
||||||||||||||||||||||
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) |