Microscopic hematuria

Symptom Information:

Symptom ID: HPO:0002907
Synonyms:
Microhematuria [HPO:0002907]
Microscopic hematuria (disorder) [Orphanet:38440]
Microscopic hematuria [Orphanet:38440]
Microscopic hematuria [OMIM:Microscopic hematuria]
Hematuria/microhematuria [Orphanet:38440]
Hematuria microscopic [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: "Microscopic hematuria" [OMIM:Microscopic 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:C0239937 "Microscopic hematuria" [Orphanet:38440]
Is a (Direct Parents):
Orphanet Abnormality of the urinary system physiology
HPO         Hematuria
MedDRA Urinary abnormalities
Orphanet Hematuria
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)
                   Abnormal urine cytology(HPO:0012614)
                      Hematuria(HPO:0000790)
                         Microscopic hematuria(HPO:0002907)
                Abnormal renal physiology(HPO:0012211)
                   Hematuria(HPO:0000790)
                      Microscopic hematuria(HPO:0002907)
             Abnormality of the upper urinary tract(HPO:0010935)
                Abnormality of the kidney(HPO:0000077)
                   Abnormal renal physiology(HPO:0012211)
                      Hematuria(HPO:0000790)
                         Microscopic hematuria(HPO:0002907)
       Abnormality of metabolism/homeostasis(HPO:0001939)
          Abnormality of urine homeostasis(HPO:0003110)
             Abnormal urine cytology(HPO:0012614)
                Hematuria(HPO:0000790)
                   Microscopic hematuria(HPO:0002907)
MedDRA:
Renal and urinary disorders(MedDRA:10038359)
    Urinary tract signs and symptoms(MedDRA:10046590)
       Urinary abnormalities(MedDRA:10000196)
          Microscopic hematuria(HPO:0002907)
Database Frequency: 27 / 7739
Resource:

All diseases associated with this symptom:

Autosomal dominant familial hematuria - retinal arteriolar tortuosity - contractures (Orphanet:73229)
Autosomal dominant progressive nephropathy with hypertension (Orphanet:88659)
CYSTINOSIS, NEPHROPATHIC (OMIM:219800)
Congenital thrombotic thrombocytopenic purpura due to ADAMTS-13 deficiency (Orphanet:93583)
Cystinosis (Orphanet:213)
Cystinuria (Orphanet:214)
Dent disease type 1 (Orphanet:93622)
Dent disease type 2 (Orphanet:93623)
EPSTEIN SYNDROME (OMIM:153650)
Fibronectin glomerulopathy (Orphanet:84090)
GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 1 (OMIM:137950)
GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 2 (OMIM:601894)
HEMATURIA, BENIGN FAMILIAL (OMIM:141200)
HERNS syndrome (Orphanet:63261)
HYDROXYPROLINEMIA (OMIM:237000)
Hereditary mucoepithelial dysplasia (Orphanet:1839)
INTERSTITIAL NEPHRITIS, KARYOMEGALIC (OMIM:614817)
IgA NEPHROPATHY, SUSCEPTIBILITY TO, 1 (OMIM:161950)
IgA NEPHROPATHY, SUSCEPTIBILITY TO, 2 (OMIM:613944)
Infundibulopelvic stenosis - multicystic kidney (Orphanet:1849)
LCAT deficiency (Orphanet:650)
Lymphangioleiomyomatosis (Orphanet:538)
NEPHROLITHIASIS, X-LINKED RECESSIVE, WITH RENAL FAILURE (OMIM:310468)
PROTEINURIA, LOW MOLECULAR WEIGHT, WITH HYPERCALCIURIA AND NEPHROCALCINOSIS (OMIM:308990)
Partial acquired lipodystrophy (Orphanet:79087)
Thrombotic thrombocytopenic purpura (Orphanet:54057)
X-linked Alport syndrome (Orphanet:88917)