{
    "disease_id": "DOID:9281", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009861", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009861", 
            "name": "folling's syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009861", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009861", 
            "name": "hyperphenylalaninemia, non-PKU mild"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009861", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009861", 
            "name": "classical phenylketonuria"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009861", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009861", 
            "name": "phenylketonuria; PKU"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009861", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009861", 
            "name": "phenylketonuria, maternal"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009861", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009861", 
            "name": "oligophrenia Phenylpyruvica"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009861", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009861", 
            "name": "imbecilitus phenylpyruvica"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009861", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009861", 
            "name": "HPA, non-PKU mild"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009861", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009861", 
            "name": "PKU"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009861", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009861", 
            "name": "Flling's disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009861", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009861", 
            "name": "phenylpyruvic oligophrenia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009861", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009861", 
            "name": "maternal phenylketonuria"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009861", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009861", 
            "name": "Folling disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009861", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009861", 
            "name": "phenylalanine hydroxylase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009861", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009861", 
            "name": "phenylalaninemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009861", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009861", 
            "name": "Pah deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:9281", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:9281", 
            "name": "Folling's disease"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:9281", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:9281", 
            "name": "PKU"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:9281", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:9281", 
            "name": "maternal phenylketonuria"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:9281", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:9281", 
            "name": "phenylalaninemia"
        }, 
        {
            "url": "https://www.omim.org/entry/261600", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:261600", 
            "name": "Hyperphenylalaninemia"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:9281", 
        "description": "An amino acid metabolic disorder that is characterized by a mutation in the gene for the hepatic enzyme phenylalanine hydroxylase (PAH), rendering it nonfunctional.", 
        "resource": "Disease Ontology", 
        "id": "DOID:9281", 
        "name": "phenylketonuria"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/261600", 
            "id": "261600", 
            "database": "MIM"
        }
    ]
}