{
    "disease_id": "DOID:0050733", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009609", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009609", 
            "name": "methylcobalamin deficiency type cblG"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009609", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009609", 
            "name": "homocystinuria-megaloblastic anemia, cblG complementation type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009609", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009609", 
            "name": "homocystinuria-megaloblastic Anemia due to defect in cobalamin metabolism, cblG complementation type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009609", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009609", 
            "name": "functional methionine synthase deficiency type cblG"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009609", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009609", 
            "name": "methylcobalamin deficiency Cbl G type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009609", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009609", 
            "name": "homocystinuria-megaloblastic anemia, cblG complementation type; HMAG"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009609", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009609", 
            "name": "methionine synthase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009609", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009609", 
            "name": "methylcobalamin deficiency, cblG type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009609", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009609", 
            "name": "cblG"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009609", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009609", 
            "name": "HMAG"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009609", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009609", 
            "name": "homocystinuria due to defect in methylation Cbl g"
        }, 
        {
            "url": "https://www.omim.org/entry/250940", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:250940", 
            "name": "Homocystinuria-megaloblastic anemia, cblG complementation type"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050733", 
        "description": "A methylmalonic acidemia that is characterized by megaloblastic anemia, lethargy, failure to thrive, developmental delay, intellectual deficit and seizures, has_material_basis_in homozygous or compound heterozygous mutation in the MTR gene on chromosome 1q43 that causes an inborn error of vitamin B12 metabolism.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050733", 
        "name": "methylmalonic aciduria and homocystinuria type cblG"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/250940", 
            "id": "250940", 
            "database": "MIM"
        }
    ]
}