Abnormal enzyme/coenzyme activity
Symptom Information:
Symptom ID: | HPO:0012379 | ||||||||
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) Abnormal enzyme/coenzyme activity(HPO:0012379) MedDRA: |
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Database Frequency: | 3 / 7739 | ||||||||
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All diseases associated with this symptom:
DEOXYRIBOSE-5-PHOSPHATE ALDOLASE DEFICIENCY | (OMIM:125460) |
Encephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome | (Orphanet:319678) |
Leigh syndrome with nephrotic syndrome | (Orphanet:255249) |