Increased urinary taurine
Symptom Information:
Symptom ID: | HPO:0003166 | ||
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 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) Aciduria(HPO:0012072) Aminoaciduria(HPO:0003355) Increased urinary taurine(HPO:0003166) Abnormality of metabolism/homeostasis(HPO:0001939) Abnormality of carboxylic acid metabolism(HPO:0004354) Abnormality of amino acid metabolism(HPO:0004337) Aminoaciduria(HPO:0003355) Increased urinary taurine(HPO:0003166) Abnormality of urine homeostasis(HPO:0003110) Aciduria(HPO:0012072) Aminoaciduria(HPO:0003355) Increased urinary taurine(HPO:0003166) MedDRA: |
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Database Frequency: | 5 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Camptodactyly of fingers | (Orphanet:295016) |
Hyper-beta-alaninemia | (Orphanet:309147) |
Hypertaurinuric cardiomyopathy | (OMIM:145350) |
Sulfite oxidase deficiency due to molybdenum cofactor deficiency type A | (Orphanet:308386) |
Sulfite oxidase deficiency due to molybdenum cofactor deficiency type B | (Orphanet:308393) |