{
    "disease_id": "DOID:0050733",
    "recommended_name": {
        "id": "DOID:0050733",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0050733",
        "name": "methylmalonic aciduria and homocystinuria type cblG",
        "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."
    },
    "synonyms": [],
    "children": [],
    "id_list": [
        "DOID:0050733"
    ],
    "unlinked_id_list": []
}