{
    "disease_id": "DOID:0111186", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013307", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013307", 
            "name": "MLASA2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013307", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013307", 
            "name": "myopathy, lactic acidosis, and sideroblastic anemia 2; MLASA2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013307", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013307", 
            "name": "YARS2 mitochondrial myopathy and sideroblastic anemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013307", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013307", 
            "name": "mitochondrial myopathy and sideroblastic anemia caused by mutation in YARS2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013307", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013307", 
            "name": "myopathy, lactic acidosis, and sideroblastic Anemia type 2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111186", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111186", 
            "name": "MLASA2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111186", 
        "description": "A myopathy, lactic acidosis, and sideroblastic anemia characterized by marked phenotypic variablity in time of onset and severity of symptoms that has_material_basis_in homozyous or compound heterozygous mutation in YARS2 on 12p11.21.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111186", 
        "name": "myopathy, lactic acidosis, and sideroblastic anemia 2"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111186#disease-associations", 
            "id": "0111186", 
            "database": "Alliance of Genome Resources"
        }
    ]
}