Showing entry for Hyperphenylalaninaemia
| General Disease Information | |
|---|---|
| BXGD Id | BXGD010440 |
| Disease Name | Hyperphenylalaninaemia |
| Disease CUI Id | C0751435 |
| MeSH Codes | C16 C18 C10 |
| Disease Class Name | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases |
| Semantic Type | Disease or Syndrome |
| Human Phenotype Ontology Id | HP:0001939 |
| Human Phenotype Ontology Term | Abnormality of metabolism/homeostasis |
| Disease Ontology Id | |
| Disease Ontology Class Name | |
| Disorder Network | disorder-protein-compound-food associations
|