{
    "disease_id": "DOID:0110738", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013674", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013674", 
            "name": "mitochondrial membrane protein-associated neurodegeneration"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013674", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013674", 
            "name": "C19orf12 neurodegeneration with brain iron accumulation"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013674", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013674", 
            "name": "neurodegeneration with brain iron accumulation 4; NBIA4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013674", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013674", 
            "name": "neurodegeneration with brain iron accumulation type 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013674", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013674", 
            "name": "neurodegeneration with brain iron accumulation due to C19orf12 mutation"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013674", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013674", 
            "name": "MPAN"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013674", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013674", 
            "name": "NBIA4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013674", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013674", 
            "name": "NBIA due to C19orf12 mutation"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013674", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013674", 
            "name": "mitochondrial Protein-associated neurodegeneration"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013674", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013674", 
            "name": "neurodegeneration with brain iron accumulation caused by mutation in C19orf12"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110738", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110738", 
            "name": "Neurodegeneration with brain iron accumulation due to C19orf12 mutation"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110738", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110738", 
            "name": "MPAN"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110738", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110738", 
            "name": "Mitochondrial Protein-Associated Neurodegeneration"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110738", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110738", 
            "name": "NBIA due to C19orf12 mutation"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110738", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110738", 
            "name": "NBIA4"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110738", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110738", 
            "name": "Neurodegeneration with brain iron accumulation type 4"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110738", 
        "description": "A neurodegeneration with brain iron accumulation that has_material_basis_in autosomal recessive inheritance of mutation in the C19orf12 gene on chromosome 19q12.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110738", 
        "name": "neurodegeneration with brain iron accumulation 4"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110738#disease-associations", 
            "id": "0110738", 
            "database": "Alliance of Genome Resources"
        }
    ]
}