Maternal hyperphenylalaninemia
Symptom Information:
| Symptom ID: | HPO:0100610 | ||||||
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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 phenylalanine metabolism(HPO:0010893) Maternal hyperphenylalaninemia(HPO:0100610) Abnormality of prenatal development or birth(HPO:0001197) Prenatal maternal abnormality(HPO:0002686) Maternal hyperphenylalaninemia(HPO:0100610) MedDRA: |
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| Database Frequency: | 1 / 7739 | ||||||
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All diseases associated with this symptom:
| Maternal hyperphenylalaninemia | (Orphanet:2209) |