Hematuria

Symptom Information:

Symptom ID: HPO:0000790
Synonyms:
Hematuria syndrome (disorder) [Orphanet:38440]
Blood in urine (finding) [Orphanet:38440]
hematuria [HPO:0000790]
Hematuria [Orphanet:38440]
Hematuria [OMIM:Hematuria]
Hematuria/microhematuria [Orphanet:38440]
Haematuria [Orphanet:38440]
Haematuria [MedDRA:10018867]
Frank haematuria [MedDRA:10018867]
Haematuria microscopic [MedDRA:10018867]
Hematuria [MedDRA:10018867]
Microscopic haematuria [MedDRA:10018867]
Urinary tract bleed microscopic [MedDRA:10018867]
Haematuria aggravated [MedDRA:10018867]
Erythrocyturia [MedDRA:10018867]
Macroscopic haematuria [MedDRA:10018867]
Macroscopic hematuria [MedDRA:10018867]
Microscopic hematuria [MedDRA:10018867]
Frank hematuria [MedDRA:10018867]
Hematuria aggravated [MedDRA:10018867]
Hematuria microscopic [MedDRA:10018867]
Chronic hematuria [MedDRA:10018867]
Chronic haematuria [MedDRA:10018867]
Glomerular haematuria [MedDRA:10018867]
Glomerular hematuria [MedDRA:10018867]
Hematuria (e.g. Hb Sarrebourg 141900.0435) [OMIM:Hematuria (e.g. Hb Sarrebourg 141900.0435)]
Hematuria (less common) [OMIM:Hematuria (less common)]
Hematuria (reported in 1 family) [OMIM:Hematuria (reported in 1 family)]
Hematuria, macroscopic (seen in children and young adults coincident with mucosal infection) [OMIM:Hematuria, macroscopic (seen in children and young adults coincident with mucosal infection)]
Hematuria, microscopic [OMIM:Hematuria, microscopic]
Microscopic hematuria. [OMIM:Microscopic hematuria.]
Quality:
Cross references:
Orphanet:38440 "Hematuria/microhematuria" [Orphanet:38440]
OMIM: "Hematuria" [OMIM:Hematuria]
OMIM: "Hematuria (e.g. Hb Sarrebourg 141900.0435)" [OMIM:Hematuria (e.g. Hb Sarrebourg 141900.0435)]
OMIM: "Hematuria (less common)" [OMIM:Hematuria (less common)]
OMIM: "Hematuria (reported in 1 family)" [OMIM:Hematuria (reported in 1 family)]
OMIM: "Hematuria, macroscopic (seen in children and young adults coincident with mucosal infection)" [OMIM:Hematuria, macroscopic (seen in children and young adults coincident with mucosal infection)]
OMIM: "Hematuria, microscopic" [OMIM:Hematuria, microscopic]
OMIM: "Microscopic hematuria." [OMIM:Microscopic hematuria.]
UMLS:C0221752 "hematuria" [HPO:0000790]
UMLS:C0018965 "Hematuria" [Orphanet:38440]
Is a (Direct Parents):
MedDRA Urinary abnormalities
HPO         Abnormal renal physiology
Orphanet Abnormality of the urinary system physiology
HPO         Abnormal urine cytology
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of metabolism/homeostasis(HPO:0001939)
          Abnormality of urine homeostasis(HPO:0003110)
             Abnormal urine cytology(HPO:0012614)
                Hematuria(HPO:0000790)
       Abnormality of the genitourinary system(HPO:0000119)
          Abnormality of the urinary system(HPO:0000079)
             Abnormality of the urinary system physiology(HPO:0011277)
                Abnormal renal physiology(HPO:0012211)
                   Hematuria(HPO:0000790)
                Abnormality of urine homeostasis(HPO:0003110)
                   Abnormal urine cytology(HPO:0012614)
                      Hematuria(HPO:0000790)
             Abnormality of the upper urinary tract(HPO:0010935)
                Abnormality of the kidney(HPO:0000077)
                   Abnormal renal physiology(HPO:0012211)
                      Hematuria(HPO:0000790)
MedDRA:
Renal and urinary disorders(MedDRA:10038359)
    Urinary tract signs and symptoms(MedDRA:10046590)
       Urinary abnormalities(MedDRA:10000196)
          Hematuria(HPO:0000790)
Database Frequency: 106 / 7739
Resource:

All diseases associated with this symptom:

AL amyloidosis (Orphanet:85443)
Adenine phosphoribosyltransferase deficiency (Orphanet:976)
Alport syndrome (Orphanet:63)
Alport syndrome - intellectual deficit - midface hypoplasia - elliptocytosis (Orphanet:86818)
Angio-osteohypertrophic syndrome (Orphanet:2346)
Anti-glomerular basement membrane disease (Orphanet:375)
Atypical hemolytic uremic syndrome with B factor anomaly (Orphanet:93578)
Atypical hemolytic uremic syndrome with C3 anomaly (Orphanet:93575)
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 beta2-microglobulinic amyloidosis (Orphanet:314652)
Autosomal dominant familial hematuria - retinal arteriolar tortuosity - contractures (Orphanet:73229)
Autosomal recessive Alport syndrome (Orphanet:88919)
BLADDER DIVERTICULUM (OMIM:109820)
Beckwith-Wiedemann syndrome due to 11p15 microdeletion (Orphanet:231127)
C3 glomerulonephritis (Orphanet:329931)
CRYOFIBRINOGENEMIA, FAMILIAL PRIMARY (OMIM:123540)
Cerebroretinal vasculopathy (Orphanet:3421)
Chronic mucocutaneous candidiasis (Orphanet:1334)
Congenital factor X deficiency (Orphanet:328)
Congenital primary megaureter (Orphanet:617)
Cryoglobulinemic vasculitis (Orphanet:91138)
Cystinuria (Orphanet:214)
Cystinuria type A (Orphanet:93612)
Cystinuria type B (Orphanet:93613)
Dense deposit disease (Orphanet:93571)
Dyschondrosteosis - nephritis (Orphanet:1765)
Ehlers-Danlos syndrome, vascular type (Orphanet:286)
Eosinophilic granulomatosis with polyangiitis (Orphanet:183)
FECHTNER SYNDROME (OMIM:153640)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS 3, SUSCEPTIBILITY TO (OMIM:607832)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS 6 (OMIM:614131)
Fabry disease (Orphanet:324)
Familial LCAT deficiency (Orphanet:79293)
Familial hypomagnesemia - hypercalciuria - nephrocalcinosis (Orphanet:31043)
Familial hypomagnesemia - hypercalciuria - nephrocalcinosis - severe ocular involvement (Orphanet:2196)
Familial renal amyloidosis (Orphanet:85450)
Fibronectin glomerulopathy (Orphanet:84090)
GLYCOGEN STORAGE DISEASE Ic (OMIM:232240)
Gaucher disease (Orphanet:355)
Gaucher disease type 1 (Orphanet:77259)
Gaucher disease type 3 (Orphanet:77261)
Giant cell arteritis (Orphanet:397)
Granulomatosis with polyangiitis (Orphanet:900)
HEMATURIA, BENIGN FAMILIAL (OMIM:141200)
HEME OXYGENASE 1 DEFICIENCY (OMIM:614034)
HEMOGLOBIN--BETA LOCUS (OMIM:141900)
HERNS syndrome (Orphanet:63261)
Hereditary hemorrhagic telangiectasia (Orphanet:774)
Hereditary mucoepithelial dysplasia (Orphanet:1839)
Hereditary neurocutaneous angioma (Orphanet:1062)
Hereditary orotic aciduria (Orphanet:30)
Hereditary vascular retinopathy (Orphanet:71291)
High myopia-sensorineural deafness syndrome (Orphanet:363396)
Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial DNA mutation (Orphanet:324525)
Hypocomplementemic urticarial vasculitis (Orphanet:36412)
Hypoparathyroidism - deafness - renal disease (Orphanet:2237)
Hypouricemia, renal, 2 (OMIM:612076)
INTERSTITIAL NEPHRITIS, KARYOMEGALIC (OMIM:614817)
IgA NEPHROPATHY, SUSCEPTIBILITY TO, 1 (OMIM:161950)
IgA NEPHROPATHY, SUSCEPTIBILITY TO, 2 (OMIM:613944)
Immunodeficiency with factor H anomaly (Orphanet:200421)
Immunoglobulin A vasculitis (Orphanet:761)
Infundibulopelvic stenosis - multicystic kidney (Orphanet:1849)
Kawasaki disease (Orphanet:2331)
Klippel-Trénaunay syndrome (Orphanet:90308)
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)
Lesch-Nyhan syndrome (Orphanet:510)
Lymphangioleiomyomatosis (Orphanet:538)
Majeed syndrome (Orphanet:77297)
Malakoplakia (Orphanet:556)
Marburg hemorrhagic fever (Orphanet:99826)
Methylmalonic acidemia with homocystinuria, type cblC (Orphanet:79282)
Microscopic polyangiitis (Orphanet:727)
Mulibrey nanism (Orphanet:2576)
Nail-patella syndrome (Orphanet:2614)
Nail-patella-like renal disease (Orphanet:2613)
Nephroblastoma (Orphanet:654)
Nephrosis - deafness - urinary tract - digital malformations (Orphanet:2669)
Oculocerebrorenal syndrome (Orphanet:534)
Partial acquired lipodystrophy (Orphanet:79087)
Pediatric systemic lupus erythematosus (Orphanet:93552)
Pierson syndrome (Orphanet:2670)
Polyarteritis nodosa, childhood-onset (OMIM:615688)
Primary hyperoxaluria (Orphanet:416)
Primary hyperoxaluria type 1 (Orphanet:93598)
Primary hyperoxaluria type 2 (Orphanet:93599)
Primary hyperoxaluria type 3 (Orphanet:93600)
Primary localized amyloidosis (Orphanet:314709)
Relapsing polychondritis (Orphanet:728)
Retinal vasculopathy and cerebral leukodystrophy (Orphanet:247691)
Rhabdoid tumor (Orphanet:69077)
Ruvalcaba syndrome (Orphanet:3121)
Scleroderma (Orphanet:801)
Senile systemic amyloidosis (Orphanet:330001)
Sickle cell anemia (Orphanet:232)
Small cell carcinoma of the bladder (Orphanet:284400)
Sweet syndrome (Orphanet:3243)
THROMBOCYTOPENIA WITH ELEVATED SERUM IgA AND RENAL DISEASE (OMIM:314000)
Transaldolase deficiency (Orphanet:101028)
Uveal coloboma - cleft lip and palate - intellectual deficit (Orphanet:1473)
Wilson disease (Orphanet:905)