{
    "disease_id": "DOID:0111557", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014906", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014906", 
            "name": "Charcot-Marie-Tooth disease, axonal, autosomal recessive, type 2a2b;"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014906", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014906", 
            "name": "CMT2A2B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014906", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014906", 
            "name": "Charcot-Marie-Tooth disease, axonal, autosomal recessive, type 2A2B; CMT2A2B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014906", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014906", 
            "name": "Charcot-Marie-Tooth disease, axonal, autosomal recessive, type 2A2B"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111557", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111557", 
            "name": "AR-CMT2, Ouvrier type"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111557", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111557", 
            "name": "autosomal recessive Charcot-Marie-Tooth disease, Ouvrier type"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111557", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111557", 
            "name": "CMT2A2B"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111557", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111557", 
            "name": "Charcot-Marie-Tooth disease, axonal, type 2A2B"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111557", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111557", 
            "name": "SEOAN due to MFN2 deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111557", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111557", 
            "name": "severe early-onset axonal neuropathy due to MFN2 deficiency"
        }, 
        {
            "url": "https://www.omim.org/entry/617087", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:617087", 
            "name": "Charcot-Marie-Tooth disease 2A2B"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111557", 
        "description": "A Charcot-Marie-Tooth disease type 2 characterized by onset of peripheral neuropathy in the first years of life that has_material_basis_in homozygous or compound heterozygous mutation in MFN2 on chromosome 1p36.22.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111557", 
        "name": "Charcot-Marie-Tooth disease type 2A2B"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/617087", 
            "id": "617087", 
            "database": "MIM"
        }
    ]
}