Proteinuria

Symptom Information:

Symptom ID: HPO:0000093
Synonyms:
Proteinuria of undiagnosed cause (disorder) [Orphanet:38400]
Proteinuria (finding) [Orphanet:38400]
Proteinuria [Orphanet:38400]
Proteinuria of undiagnosed cause [Orphanet:38400]
Proteinuria [OMIM:Proteinuria]
Proteinuria [MedDRA:10037032]
Proteinuria present [MedDRA:10037032]
Proteinuria aggravated [MedDRA:10037032]
Proteinuria-aggravated [MedDRA:10037032]
Proteinuria (in 2 of 3 siblings) [OMIM:Proteinuria (in 2 of 3 siblings)]
Proteinuria (rare) [OMIM:Proteinuria (rare)]
Proteinuria (type II, congenital) [OMIM:Proteinuria (type II, congenital)]
Quality:
Cross references:
Orphanet:38400 "Proteinuria" [Orphanet:38400]
OMIM: "Proteinuria" [OMIM:Proteinuria]
OMIM: "Proteinuria (in 2 of 3 siblings)" [OMIM:Proteinuria (in 2 of 3 siblings)]
OMIM: "Proteinuria (rare)" [OMIM:Proteinuria (rare)]
OMIM: "Proteinuria (type II, congenital)" [OMIM:Proteinuria (type II, congenital)]
UMLS:C0033687 "Proteinuria" [Orphanet:38400]
UMLS:C1279888 "Proteinuria of undiagnosed cause" [Orphanet:38400]
Is a (Direct Parents):
Orphanet Abnormality of the urinary system physiology
MedDRA Urinary abnormalities
HPO         Bence Jones Proteinuria
HPO         Abnormality of urine homeostasis
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of metabolism/homeostasis(HPO:0001939)
          Abnormality of urine homeostasis(HPO:0003110)
             Proteinuria(HPO:0000093)
       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)
MedDRA:
Renal and urinary disorders(MedDRA:10038359)
    Urinary tract signs and symptoms(MedDRA:10046590)
       Urinary abnormalities(MedDRA:10000196)
          Proteinuria(HPO:0000093)
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)