{
    "disease_id": "DOID:0080580", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008862", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008862", 
            "name": "methylcrotonylglycinuria, type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008862", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008862", 
            "name": "MCCC2 3-methylcrotonyl-CoA carboxylase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008862", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008862", 
            "name": "MCC 2 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008862", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008862", 
            "name": "MCC2D"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008862", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008862", 
            "name": "3-methylcrotonylglycinuria 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008862", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008862", 
            "name": "3-methylcrotonyl-CoA carboxylase deficiency caused by mutation in MCCC2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008862", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008862", 
            "name": "3 alpha methylcrotonyl-CoA carboxylase 2 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008862", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008862", 
            "name": "MCC2 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008862", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008862", 
            "name": "3-METHYLCROTONYL-CoA carboxylase 2 deficiency; MCC2D"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008862", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008862", 
            "name": "3 alpha methylcrotonylglycinuria 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008862", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008862", 
            "name": "methylcrotonylglycinuria type 2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080580", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080580", 
        "name": "3-Methylcrotonyl-CoA carboxylase 2 deficiency"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080580#disease-associations", 
            "id": "0080580", 
            "database": "Alliance of Genome Resources"
        }
    ]
}