Abnormal urinary color
Symptom Information:
Symptom ID: | HPO:0012086 | ||||||||||||||||||||||||||||||
Synonyms: |
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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 urinary color(HPO:0012086) 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 urinary color(HPO:0012086) MedDRA: Renal and urinary disorders(MedDRA:10038359) Urinary tract signs and symptoms(MedDRA:10046590) Urinary abnormalities(MedDRA:10000196) Abnormal urinary color(HPO:0012086) |
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Database Frequency: | 19 / 7739 | ||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Acute intermittent porphyria | (Orphanet:79276) |
Alkaptonuria | (Orphanet:56) |
Autoimmune hemolytic anemia | (Orphanet:98375) |
Autoimmune hemolytic anemia, warm type | (Orphanet:90033) |
Benign recurrent intrahepatic cholestasis | (Orphanet:65682) |
Blue diaper syndrome | (Orphanet:94086) |
Cholangiocarcinoma | (Orphanet:70567) |
Cholestasis - lymphedema | (Orphanet:1414) |
Choreoacanthocytosis | (Orphanet:2388) |
Cold agglutinin disease | (Orphanet:56425) |
Congenital erythropoietic porphyria | (Orphanet:79277) |
Drug-induced autoimmune hemolytic anemia | (Orphanet:90037) |
Dubin-Johnson syndrome | (Orphanet:234) |
Hartnup syndrome | (Orphanet:2116) |
Lymphangioleiomyomatosis | (Orphanet:538) |
MYOPATHY DUE TO MALATE-ASPARTATE SHUTTLE DEFECT | (OMIM:254960) |
Mixed-type autoimmune hemolytic anemia | (Orphanet:90036) |
Paroxysmal cold hemoglobinuria | (Orphanet:90035) |
Porphyria | (Orphanet:738) |