{
    "disease_id": "DOID:0080579", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008861", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008861", 
            "name": "deficiency of methylcrotonoyl-Coa carboxylase"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008861", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008861", 
            "name": "MCC1D"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008861", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008861", 
            "name": "methylcrotonylglycinuria type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008861", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008861", 
            "name": "3 alpha methylcrotonylglycinuria 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008861", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008861", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008861", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008861", 
            "name": "MCCC1 3-methylcrotonyl-CoA carboxylase deficiency"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008861", 
            "name": "3 Methylcrotonyl-CoA carboxylase 1 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008861", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008861", 
            "name": "MCC deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008861", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008861", 
            "name": "3-methylcrotonylglycinuria 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008861", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008861", 
            "name": "3-Methylcrotonyl-Coa carboxylase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008861", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008861", 
            "name": "3-methylcrotonyl-CoA carboxylase deficiency caused by mutation in MCCC1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008861", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008861", 
            "name": "3-methylcrotonylglycinuria"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008861", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008861", 
            "name": "methylcrotonoyl-CoA carboxylase 1 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008861", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008861", 
            "name": "Mcc1 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008861", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008861", 
            "name": "3 methylcrotonylglycinuria"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008861", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008861", 
            "name": "3-MCC deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008861", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008861", 
            "name": "methylcrotonylglycinuria type I"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008861", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008861", 
            "name": "Mccd type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008861", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008861", 
            "name": "3-Methylcrotonyl-Coenzyme A carboxylase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008861", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008861", 
            "name": "3-METHYLCROTONYL-CoA carboxylase 1 deficiency; MCC1D"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008861", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008861", 
            "name": "MCC 1 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008861", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008861", 
            "name": "Methylcrotonyl-Coa carboxylase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008861", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008861", 
            "name": "3 Methylcrotonyl-CoA carboxylase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008861", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008861", 
            "name": "3-methylcrotonylglycinuria I"
        }, 
        {
            "url": "https://www.omim.org/entry/210200", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:210200", 
            "name": "3-methylcrotonoyl-CoA carboxylase 1 deficiency"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080579", 
        "description": "A 3-Methylcrotonyl-CoA carboxylase deficiency that has_material_basis_in  homozygous or compound heterozygous mutation in the gene encoding the alpha subunit of 3-methylcrotonyl-CoA carboxylase on chromosome 3q27.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080579", 
        "name": "3-Methylcrotonyl-CoA carboxylase 1 deficiency"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/210200", 
            "id": "210200", 
            "database": "MIM"
        }
    ]
}