{
    "disease_id": "DOID:0111184", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010782", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010782", 
            "name": "MLASA3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010782", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010782", 
            "name": "myopathy, lactic acidosis, and sideroblastic anemia 3; MLASA3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010782", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010782", 
            "name": "myopathy, lactic acidosis, and sideroblastic anemia type 3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111184", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111184", 
            "name": "MLASA3"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111184", 
        "description": "A myopathy, lactic acidosis, and sideroblastic anemia characterized by early infantile onset of transfusion-dependent sideroblastic anemia with failure to thrive, hearing loss, epilepsy, stroke-like episodes, and severe developmental delay that has_material_basis_in heteroplasmic mutation in MTATP6 encoded by nucleotides 8527-9207 of the mitochondrial genome.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111184", 
        "name": "myopathy, lactic acidosis, and sideroblastic anemia 3"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/500011", 
            "id": "500011", 
            "database": "MIM"
        }
    ]
}