{
    "disease_id": "DOID:0050716",
    "recommended_name": {
        "id": "DOID:0050716",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0050716",
        "name": "methylmalonic aciduria and homocystinuria type cblD",
        "description": "A methylmalonic aciduria that is characterized by combined homocystinuria and methylmalonic aciduria and deficiency of MCM and MS activities."
    },
    "synonyms": [
        {
            "id": "DOID:0050716",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0050716",
            "name": "Cobalamin D deficiency",
            "description": ""
        },
        {
            "id": "DOID:0050716",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0050716",
            "name": "MAHCD",
            "description": ""
        },
        {
            "id": "MONDO:0010185",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010185",
            "name": "methylmalonic aciduria and homocystinuria type cblD",
            "description": "A form of methylmalonic acidemia with homocystinuria, an inborn error of vitamin B12 (cobalamin) metabolism characterized by variable biochemical, neurological and hematological manifestations."
        },
        {
            "id": "MONDO:0010185",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010185",
            "name": "cblD defect",
            "description": ""
        },
        {
            "id": "MONDO:0010185",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010185",
            "name": "cobalamin D defect",
            "description": ""
        },
        {
            "id": "MONDO:0010185",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010185",
            "name": "cobalamin d disease",
            "description": ""
        },
        {
            "id": "MONDO:0010185",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010185",
            "name": "combined defect in adenosylcobalamin and methylcobalamin synthesis, type cblD",
            "description": ""
        },
        {
            "id": "MONDO:0010185",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010185",
            "name": "methylmalonic aciduria and homocystinuria type cblD",
            "description": ""
        },
        {
            "id": "MONDO:0010185",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010185",
            "name": "methylmalonic aciduria with homocystinuria, type cblD",
            "description": ""
        },
        {
            "id": "MONDO:0010185",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010185",
            "name": "MAHCD",
            "description": ""
        },
        {
            "id": "MONDO:0010185",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010185",
            "name": "homocystinuria, cblD type, variant 1, included",
            "description": ""
        },
        {
            "id": "MONDO:0010185",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010185",
            "name": "mehtylmalonic acidemia with homocystinuria cbI d",
            "description": ""
        },
        {
            "id": "MONDO:0010185",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010185",
            "name": "methylmalonic acidemia with homocystinuria type cblD",
            "description": ""
        },
        {
            "id": "MONDO:0010185",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010185",
            "name": "methylmalonic acidemia, Cblh type",
            "description": ""
        },
        {
            "id": "MONDO:0010185",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010185",
            "name": "methylmalonic aciduria, Cblh type",
            "description": ""
        },
        {
            "id": "MONDO:0010185",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010185",
            "name": "methylmalonic aciduria, cblD type, variant 2, included",
            "description": ""
        },
        {
            "id": "MIM:277410",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/277410",
            "name": "Methylmalonic aciduria and homocystinuria, cblD type",
            "description": "Methylmalonic aciduria and homocystinuria, cblD type"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0050716"
    ],
    "unlinked_id_list": []
}