Microscopic hematuria
Symptom Information:
Symptom ID: | HPO:0002907 | ||||||||||||||||||||||||||||||
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 metabolism/homeostasis(HPO:0001939) Abnormality of urine homeostasis(HPO:0003110) Abnormal urine cytology(HPO:0012614) Hematuria(HPO:0000790) Microscopic hematuria(HPO:0002907) 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) Microscopic hematuria(HPO:0002907) Abnormality of urine homeostasis(HPO:0003110) Abnormal urine cytology(HPO:0012614) 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) MedDRA: Renal and urinary disorders(MedDRA:10038359) Urinary tract signs and symptoms(MedDRA:10046590) Urinary abnormalities(MedDRA:10000196) Microscopic hematuria(HPO:0002907) |
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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) |