{
    "disease_id": "DOID:0111270", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010089", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010089", 
            "name": "sulfite oxidase deficiency, isolated; ISOD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010089", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010089", 
            "name": "sulfite oxidase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010089", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010089", 
            "name": "sulfite oxidase deficiency, isolated"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010089", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010089", 
            "name": "Sulfocysteinuria"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010089", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010089", 
            "name": "ISOD"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111270", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111270", 
            "name": "sulfocysteinuria"
        }, 
        {
            "url": "https://www.omim.org/entry/272300", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:272300", 
            "name": "Sulfite oxidase deficiency, isolated"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111270", 
        "description": "An inherited metabolic disorder characterized by increased sulfite in the urine with markedly decreased inorganic sulfate excretion and resulting in variable phenotypes ranging from severe early onset disease to late-onset, milder disease that has_material_basis_in homozygous or compound heterozygous mutation in SUOX on 12q13.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111270", 
        "name": "isolated sulfite oxidase deficiency"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/272300", 
            "id": "272300", 
            "database": "MIM"
        }
    ]
}