Proteinuria
Symptom Information:
Symptom ID: | HPO:0000093 | ||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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 urinary system physiology(HPO:0011277) Abnormality of urine homeostasis(HPO:0003110) Proteinuria(HPO:0000093) Abnormality of metabolism/homeostasis(HPO:0001939) Abnormality of urine homeostasis(HPO:0003110) Proteinuria(HPO:0000093) MedDRA: Renal and urinary disorders(MedDRA:10038359) Urinary tract signs and symptoms(MedDRA:10046590) Urinary abnormalities(MedDRA:10000196) Proteinuria(HPO:0000093) |
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Database Frequency: | 169 / 7739 | ||||||||||||
Resource: |
All diseases associated with this symptom:
AA amyloidosis | (Orphanet:85445) |
Action myoclonus - renal failure syndrome | (Orphanet:163696) |
Alport syndrome | (Orphanet:63) |
Alport syndrome - intellectual deficit - midface hypoplasia - elliptocytosis | (Orphanet:86818) |
Alström syndrome | (Orphanet:64) |
Anti-glomerular basement membrane disease | (Orphanet:375) |
Arthrogryposis - renal dysfunction - cholestasis | (Orphanet:2697) |
Atherosclerosis - deafness - diabetes - epilepsy - nephropathy | (Orphanet:1192) |
Atypical hemolytic uremic syndrome with B factor anomaly | (Orphanet:93578) |
Atypical hemolytic uremic syndrome with C3 anomaly | (Orphanet:93575) |
Atypical hemolytic uremic syndrome with DGKE deficiency | (Orphanet:357008) |
Atypical hemolytic uremic syndrome with I factor anomaly | (Orphanet:93580) |
Atypical hemolytic uremic syndrome with MCP/CD46 anomaly | (Orphanet:93576) |
Atypical hemolytic uremic syndrome with thrombomodulin anomaly | (Orphanet:217023) |
Autosomal dominant Alport syndrome | (Orphanet:88918) |
Autosomal dominant beta2-microglobulinic amyloidosis | (Orphanet:314652) |
Autosomal dominant intermediate Charcot-Marie-Tooth disease type E | (Orphanet:93114) |
Autosomal dominant progressive nephropathy with hypertension | (Orphanet:88659) |
Autosomal recessive Alport syndrome | (Orphanet:88919) |
BILIARY MALFORMATION WITH RENAL TUBULAR INSUFFICIENCY | (OMIM:210550) |
Bardet-Biedl syndrome 2 | (OMIM:615981) |
Bilateral renal agenesis | (Orphanet:1848) |
Blepharophimosis-intellectual deficit syndrome, Ohdo type | (Orphanet:2728) |
CEDNIK syndrome | (Orphanet:66631) |
CHONDROITIN-6-SULFATURIA, DEFECTIVE CELLULAR IMMUNITY, NEPHROTIC SYNDROME | (OMIM:215250) |
COCKAYNE SYNDROME A | (OMIM:216400) |
COCKAYNE SYNDROME B | (OMIM:133540) |
COCKAYNE SYNDROME, TYPE III | (OMIM:216411) |
COENZYME Q10 DEFICIENCY, PRIMARY, 3 | (OMIM:614652) |
CORNELIA DE LANGE SYNDROME 1 | (OMIM:122470) |
CYSTINOSIS, LATE-ONSET JUVENILE OR ADOLESCENT NEPHROPATHIC TYPE | (OMIM:219900) |
CYSTINOSIS, NEPHROPATHIC | (OMIM:219800) |
Castleman disease | (Orphanet:160) |
Cerebroretinal vasculopathy | (Orphanet:3421) |
Cockayne syndrome | (Orphanet:191) |
Congenital nephrotic syndrome, Finnish type | (Orphanet:839) |
Congenital thrombotic thrombocytopenic purpura due to ADAMTS-13 deficiency | (Orphanet:93583) |
Cornelia de Lange syndrome | (Orphanet:199) |
Cryoglobulinemic vasculitis | (Orphanet:91138) |
Cystinosis | (Orphanet:213) |
Deafness - intellectual deficit, Martin-Probst type | (Orphanet:85321) |
Denys-Drash syndrome | (Orphanet:220) |
Diffuse cutaneous systemic sclerosis | (Orphanet:220393) |
Distal limb deficiencies - micrognathia syndrome | (Orphanet:1307) |
Donnai-Barrow syndrome | (Orphanet:2143) |
Dyschondrosteosis - nephritis | (Orphanet:1765) |
EPSTEIN SYNDROME | (OMIM:153650) |
Ebola hemorrhagic fever | (Orphanet:319218) |
Eosinophilic granulomatosis with polyangiitis | (Orphanet:183) |
FAMILIAL MEDITERRANEAN FEVER, AUTOSOMAL DOMINANT | (OMIM:134610) |
FANCONI RENOTUBULAR SYNDROME 2 | (OMIM:613388) |
FECHTNER SYNDROME | (OMIM:153640) |
FOCAL SEGMENTAL GLOMERULOSCLEROSIS 1 | (OMIM:603278) |
FOCAL SEGMENTAL GLOMERULOSCLEROSIS 2 | (OMIM:603965) |
FOCAL SEGMENTAL GLOMERULOSCLEROSIS 3, SUSCEPTIBILITY TO | (OMIM:607832) |
FOCAL SEGMENTAL GLOMERULOSCLEROSIS 6 | (OMIM:614131) |
FOCAL SEGMENTAL GLOMERULOSCLEROSIS 7 | (OMIM:616002) |
FOCAL SEGMENTAL GLOMERULOSCLEROSIS 8 | (OMIM:616032) |
Fabry disease | (Orphanet:324) |
Familial LCAT deficiency | (Orphanet:79293) |
Familial Mediterranean fever | (Orphanet:342) |
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) |
Fanconi renotubular syndrome 1 | (OMIM:134600) |
Fibronectin glomerulopathy | (Orphanet:84090) |
Frasier syndrome | (Orphanet:347) |
Free sialic acid storage disease | (Orphanet:834) |
GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 1 | (OMIM:137950) |
GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 2 | (OMIM:601894) |
GLYCOGEN STORAGE DISEASE Ic | (OMIM:232240) |
Galloway-Mowat syndrome | (Orphanet:2065) |
Gaucher disease | (Orphanet:355) |
Gaucher disease type 1 | (Orphanet:77259) |
Gaucher disease type 3 | (Orphanet:77261) |
Glycogen storage disease due to glucose-6-phosphatase deficiency | (Orphanet:364) |
Glycogen storage disease due to glucose-6-phosphatase deficiency type a | (Orphanet:79258) |
Glycogen storage disease due to glucose-6-phosphatase deficiency type b | (Orphanet:79259) |
Granulomatosis with polyangiitis | (Orphanet:900) |
Gräsbeck-Imerslund disease | (Orphanet:35858) |
HEME OXYGENASE 1 DEFICIENCY | (OMIM:614034) |
HERNS syndrome | (Orphanet:63261) |
Hemorrhagic fever - renal syndrome | (Orphanet:340) |
Hereditary vascular retinopathy | (Orphanet:71291) |
High myopia-sensorineural deafness syndrome | (Orphanet:363396) |
Holoprosencephaly | (Orphanet:2162) |
Hydrocephalus - blue sclerae - nephropathy | (Orphanet:2186) |
Hyperprolinemia type 1 | (Orphanet:419) |
Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial DNA mutation | (Orphanet:324525) |
Hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome | (Orphanet:363694) |
Hypocomplementemic urticarial vasculitis | (Orphanet:36412) |
Hypoparathyroidism - deafness - renal disease | (Orphanet:2237) |
INTERSTITIAL NEPHRITIS, KARYOMEGALIC | (OMIM:614817) |
Idiopathic hypereosinophilic syndrome | (Orphanet:3260) |
IgA NEPHROPATHY, SUSCEPTIBILITY TO, 1 | (OMIM:161950) |
IgA NEPHROPATHY, SUSCEPTIBILITY TO, 2 | (OMIM:613944) |
Immunoglobulin A vasculitis | (Orphanet:761) |
Immunoglobulin-mediated membranoproliferative glomerulonephritis | (Orphanet:329903) |
Insulin-resistance syndrome type A | (Orphanet:2297) |
Isolated cytochrome C oxidase deficiency | (Orphanet:254905) |
Jeune syndrome | (Orphanet:474) |
Kawasaki disease | (Orphanet:2331) |
LAMB-2-related infantile-onset nephrotic syndrome | (Orphanet:306507) |
LCAT deficiency | (Orphanet:650) |
LEIOMYOMATOSIS, DIFFUSE, WITH ALPORT SYNDROME | (OMIM:308940) |
LIPODYSTROPHY, PARTIAL, ACQUIRED, WITH LOW COMPLEMENT COMPONENT C3,WITH OR WITHOUT GLOMERULONEPHRITIS | (OMIM:613913) |
Legionellosis | (Orphanet:549) |
Leigh syndrome with nephrotic syndrome | (Orphanet:255249) |
Leprechaunism | (Orphanet:508) |
Limited cutaneous systemic sclerosis | (Orphanet:220402) |
Limited systemic sclerosis | (Orphanet:220407) |
Lipoprotein glomerulopathy | (Orphanet:329481) |
Lymphedema - distichiasis | (Orphanet:33001) |
MELAS | (Orphanet:550) |
Majeed syndrome | (Orphanet:77297) |
Malakoplakia | (Orphanet:556) |
Maternally-inherited diabetes and deafness | (Orphanet:225) |
Maturity-onset diabetes of the young, type 2 | (OMIM:125851) |
Methylmalonic acidemia with homocystinuria, type cblC | (Orphanet:79282) |
Mu heavy-chain disease | (Orphanet:100024) |
Multicentric carpo-tarsal osteolysis with or without nephropathy | (Orphanet:2774) |
NEPHROTIC SYNDROME, TYPE 2 | (OMIM:600995) |
NEPHROTIC SYNDROME, TYPE 3 | (OMIM:610725) |
NEPHROTIC SYNDROME, TYPE 8 | (OMIM:615244) |
NEPHROTIC SYNDROME, TYPE 9 | (OMIM:615573) |
Nail-patella syndrome | (Orphanet:2614) |
Nail-patella-like renal disease | (Orphanet:2613) |
Nephropathy - deafness - hyperparathyroidism | (Orphanet:2668) |
Nephrosis - deafness - urinary tract - digital malformations | (Orphanet:2669) |
Oculo-reno-cerebellar syndrome | (Orphanet:2715) |
Oculo-skeletal-renal syndrome | (Orphanet:2716) |
Oculocerebrorenal syndrome | (Orphanet:534) |
Orofaciodigital syndrome type 1 | (Orphanet:2750) |
PHEOCHROMOCYTOMA--ISLET CELL TUMOR SYNDROME | (OMIM:171420) |
PHEOCHROMOCYTOMAPHEOCHROMOCYTOMA, SUSCEPTIBILITY TO | (OMIM:171300) |
PMM2-CDG | (Orphanet:79318) |
PREECLAMPSIA/ECLAMPSIA 1 | (OMIM:189800) |
Partial acquired lipodystrophy | (Orphanet:79087) |
Pearson syndrome | (Orphanet:699) |
Pediatric systemic lupus erythematosus | (Orphanet:93552) |
Pediatric systemic sclerosis | (Orphanet:93567) |
Pierson syndrome | (Orphanet:2670) |
Polyarteritis nodosa, childhood-onset | (OMIM:615688) |
Preeclampsia | (Orphanet:275555) |
Primary Fanconi syndrome | (Orphanet:3337) |
Pyogenic arthritis - pyoderma gangrenosum - acne | (Orphanet:69126) |
Rabson-Mendenhall syndrome | (Orphanet:769) |
Relapsing polychondritis | (Orphanet:728) |
Renal coloboma syndrome | (Orphanet:1475) |
Renal cysts and diabetes syndrome | (Orphanet:93111) |
Retinal ischemic syndrome - digestive tract small vessel hyalinosis - diffuse cerebral calcifications | (Orphanet:3018) |
Retinal vasculopathy and cerebral leukodystrophy | (Orphanet:247691) |
Schimke immuno-osseous dysplasia | (Orphanet:1830) |
Short-rib thoracic dysplasia 1 with or without polydactyly | (OMIM:208500) |
Short-rib thoracic dysplasia 5 with or without polydactyly | (OMIM:614376) |
Sialidosis type 1 | (Orphanet:812) |
Siegler-Brewer-Carey syndrome | (Orphanet:3167) |
Spastic paraplegia - nephritis - deafness | (Orphanet:2820) |
Sweet syndrome | (Orphanet:3243) |
Thrombotic thrombocytopenic purpura | (Orphanet:54057) |
Torticollis - keloids - cryptorchidism - renal dysplasia | (Orphanet:3341) |
Transaldolase deficiency | (Orphanet:101028) |
Tyrosinemia type 1 | (Orphanet:882) |
Williams syndrome | (Orphanet:904) |
Wilson disease | (Orphanet:905) |
X-linked Alport syndrome | (Orphanet:88917) |
Yellow fever | (Orphanet:99829) |
[DEL] GLYCOGEN STORAGE DISEASE Ib | (OMIM:232220) |