Hyposerinemia
Symptom Information:
| Symptom ID: | HPO:0012279 | ||
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| Is a (Whole tree): |
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 serine family amino acid metabolism(HPO:0010894) Abnormality of serine metabolism(HPO:0012278) Hyposerinemia(HPO:0012279) MedDRA: |
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| Database Frequency: | 1 / 7739 | ||
| Resource: |
All diseases associated with this symptom:
| Phosphoserine aminotransferase deficiency | (Orphanet:284417) |