Hematuria
Symptom Information:
Symptom ID: | HPO:0000790 | |||||||||||||||||||||||||||||||
Synonyms: |
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Quality: | ||||||||||||||||||||||||||||||||
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 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) |
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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) |