{
    "disease_id": "DOID:0060740", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009612", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009612", 
            "name": "vitamin B12-unresponsive methylmalonic aciduria"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009612", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009612", 
            "name": "methylmalonic aciduria, mut type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009612", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009612", 
            "name": "methylmalonic aciduria, mut(0) type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009612", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009612", 
            "name": "methylmalonic aciduria, mut(-) type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009612", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009612", 
            "name": "methylmalonic acidemia due to methylmalonyl-Coa mutase deficiency MMA due to MCM deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009612", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009612", 
            "name": "methylmalonyl-CoA mutase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009612", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009612", 
            "name": "methylmalonic acidemia due to methylmalonyl-CoA mutase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009612", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009612", 
            "name": "MCM deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009612", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009612", 
            "name": "methylmalonic aciduria mut type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009612", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009612", 
            "name": "methylmalonyl-Coenzyme A mutase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009612", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009612", 
            "name": "vitamin B12-unresponsive methylmalonic acidemia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060740", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060740", 
            "name": "methylmalonic aciduria mut type"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060740", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060740", 
            "name": "vitamin B12-unresponsive methylmalonic aciduria"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060740", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060740", 
            "name": "methylmalonic acidemia due to methylmalonyl-CoA mutase deficiency"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060740", 
        "description": "A methylmalonic acidemia characterized by accumulation of methylmalonic acid in the blood that is unresponsive to vitamn B12 therapy and that has_material_basis_in mutation in the MUT gene on chromosome 6p12.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060740", 
        "name": "methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060740#disease-associations", 
            "id": "0060740", 
            "database": "Alliance of Genome Resources"
        }
    ]
}