{
    "disease_id": "DOID:0080580",
    "recommended_name": {
        "id": "DOID:0080580",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0080580",
        "name": "3-Methylcrotonyl-CoA carboxylase 2 deficiency",
        "description": "A 3-Methylcrotonyl-CoA carboxylase deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the gene encoding the beta subunit of 3-methylcrotonyl-CoA carboxylase on chromosome 5q13."
    },
    "synonyms": [
        {
            "id": "MONDO:0008862",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008862",
            "name": "3-methylcrotonyl-CoA carboxylase 2 deficiency",
            "description": "Any 3-methylcrotonyl-CoA carboxylase deficiency in which the cause of the disease is a mutation in the MCCC2 gene."
        },
        {
            "id": "MONDO:0008862",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008862",
            "name": "methylcrotonylglycinuria, type 2",
            "description": ""
        },
        {
            "id": "MONDO:0008862",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008862",
            "name": "MCCC2 3-methylcrotonyl-CoA carboxylase deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0008862",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008862",
            "name": "MCC 2 deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0008862",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008862",
            "name": "MCC2D",
            "description": ""
        },
        {
            "id": "MONDO:0008862",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008862",
            "name": "3-methylcrotonylglycinuria 2",
            "description": ""
        },
        {
            "id": "MONDO:0008862",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008862",
            "name": "3-methylcrotonyl-CoA carboxylase deficiency caused by mutation in MCCC2",
            "description": ""
        },
        {
            "id": "MONDO:0008862",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008862",
            "name": "3-Methylcrotonyl-CoA carboxylase 2 deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0008862",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008862",
            "name": "3 alpha methylcrotonyl-CoA carboxylase 2 deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0008862",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008862",
            "name": "MCC2 deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0008862",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008862",
            "name": "3-METHYLCROTONYL-CoA carboxylase 2 deficiency; MCC2D",
            "description": ""
        },
        {
            "id": "MONDO:0008862",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008862",
            "name": "3 alpha methylcrotonylglycinuria 2",
            "description": ""
        },
        {
            "id": "MONDO:0008862",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008862",
            "name": "methylcrotonylglycinuria type 2",
            "description": ""
        },
        {
            "id": "MIM:210210",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/210210",
            "name": "3-methylcrotonoyl-CoA carboxylase 2 deficiency",
            "description": "3-methylcrotonoyl-CoA carboxylase 2 deficiency"
        }
    ]
}