{
    "disease_id": "DOID:0111185", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024553", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024553", 
            "name": "PUS1 myopathy, lactic acidosis, and sideroblastic anemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024553", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024553", 
            "name": "mitochondrial myopathy and sideroblastic anemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024553", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024553", 
            "name": "MLASA1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024553", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024553", 
            "name": "myopathy, lactic acidosis, and sideroblastic anemia caused by mutation in PUS1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024553", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024553", 
            "name": "myopathy, lactic acidosis, and sideroblastic anemia 1; MLASA1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111185", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111185", 
            "name": "MLASA1"
        }, 
        {
            "url": "https://www.omim.org/entry/600462", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:600462", 
            "name": "Myopathy with lactic acidosis and sideroblastic anemia 1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111185", 
        "description": "A myopathy, lactic acidosis, and sideroblastic anemia that has_material_basis_in homozygous or compound heterozygous mutation in PUS1 on 12q24.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111185", 
        "name": "myopathy, lactic acidosis, and sideroblastic anemia 1"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/600462", 
            "id": "600462", 
            "database": "MIM"
        }
    ]
}