{
    "disease_id": "DOID:0110003", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014561", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014561", 
            "name": "3-methylglutaconic aciduria type 7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014561", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014561", 
            "name": "3-methylglutaconic aciduria type VII"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014561", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014561", 
            "name": "3-methylglutaconic aciduria caused by mutation in CLPB"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014561", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014561", 
            "name": "3-METHYLGLUTACONIC aciduria with cataracts, neurologic involvement, and neutropenia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014561", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014561", 
            "name": "MGA7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014561", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014561", 
            "name": "3-Methylglutaconic aciduria, type 7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014561", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014561", 
            "name": "MGCA7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014561", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014561", 
            "name": "3-methylglutaconic aciduria-cataract-neurologic involvement-neutropenia syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014561", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014561", 
            "name": "CLPB 3-methylglutaconic aciduria"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014561", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014561", 
            "name": "3-METHYLGLUTACONIC aciduria with cataracts, neurologic involvement, and neutropenia; MEGCANN"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014561", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014561", 
            "name": "MEGCANN"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110003", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110003", 
            "name": "3-methylglutaconic aciduria type 7"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110003", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110003", 
            "name": "3-methylglutaconic aciduria type VII"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110003", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110003", 
            "name": "MEGCANN"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110003", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110003", 
            "name": "MGA7"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110003", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110003", 
            "name": "MGCA7"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110003", 
        "description": "A 3-methylglutaconic aciduria that has_material_basis_in homozygous or compound heterozygous mutation in the CLPB gene on chromosome 11q13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110003", 
        "name": "3-methylglutaconic aciduria with cataracts, neurologic involvement and neutropenia"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110003#disease-associations", 
            "id": "0110003", 
            "database": "Alliance of Genome Resources"
        }
    ]
}