Human Gene Set: HP_TRANSIENT_HYPERPHENYLALANINEMIA


Standard name HP_TRANSIENT_HYPERPHENYLALANINEMIA
Systematic name M46134
Brief description Transient hyperphenylalaninemia
Full description or abstract A condition of not having consistently high levels of phenylalanine in the blood but of experiencing temporary hyperphenylalaninemia following ingestion of large quantities of phenylalanine (for instance, following an oral loading test with phenylalanine). [https://orcid.org/0000-0002-0736-9199]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0008297
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0008297
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Source species Homo sapiens
Contributed by Human Phenotype Ontology Group (The Jackson Laboratory (JAX))
Source platform or
identifier namespace		 Human_NCBI_Gene_ID
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Version history 2026.1.Hs: Updated to HPO Release 2026-01-08.


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