Abnormality of tryptophan metabolism
Symptom Information:
| Symptom ID: | HPO:0004365 | ||
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HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of metabolism/homeostasis(HPO:0001939) Abnormality of carboxylic acid metabolism(HPO:0004354) Abnormality of amino acid metabolism(HPO:0004337) Abnormality of aromatic amino acid family metabolism(HPO:0004338) Abnormality of tryptophan metabolism(HPO:0004365) MedDRA: |
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| Database Frequency: | 4 / 7739 | ||
| Resource: |
All diseases associated with this symptom:
| Blue diaper syndrome | (Orphanet:94086) |
| Dyschromatosis universalis hereditaria 1 | (OMIM:127500) |
| Dyschromatosis universalis hereditaria 2 | (OMIM:612715) |
| Dyschromatosis universalis hereditaris 3 | (OMIM:615402) |