Maternal hyperphenylalaninemia

Symptom Information:

Symptom ID: HPO:0100610
Synonyms:
Maternal hyperphenylalaninemia [Orphanet:55640]
Quality:
Cross references:
Orphanet:55640 "Maternal hyperphenylalaninemia" [Orphanet:55640]
Is a (Direct Parents):
HPO         Abnormality of phenylalanine metabolism
HPO         Prenatal maternal abnormality
Orphanet Abnormality of prenatal development or birth
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of prenatal development or birth(HPO:0001197)
          Prenatal maternal abnormality(HPO:0002686)
             Maternal hyperphenylalaninemia(HPO:0100610)
       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)
MedDRA:
Database Frequency: 1 / 7739
Resource:

All diseases associated with this symptom:

Maternal hyperphenylalaninemia (Orphanet:2209)