{
    "disease_id": "DOID:0111629", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009111", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009111", 
            "name": "dihydropyrimidinuria"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009111", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009111", 
            "name": "Dpys deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009111", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009111", 
            "name": "dihydropyrimidinase deficiency; DPYSD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009111", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009111", 
            "name": "Dph deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009111", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009111", 
            "name": "DPYSD"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111629", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111629", 
            "name": "DPH deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111629", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111629", 
            "name": "DPYS deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111629", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111629", 
            "name": "DPYSD"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111629", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111629", 
            "name": "dihydropyrimidinuria"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111629", 
        "description": "A pyrimidine metabolic disorder characterized by a defect in the degredation of uracil and thymine resulting in elevated levels of 5,6-dihydrouracil and 5,6-dihydrothymine in urine that has_material_basis_in homozygous or compound heterozygous mutation in DPYS on chromosome 8q22.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111629", 
        "name": "dihydropyrimidinase deficiency"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/222748", 
            "id": "222748", 
            "database": "MIM"
        }
    ]
}