{
    "disease_id": "DOID:0110166",
    "recommended_name": {
        "id": "DOID:0110166",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110166",
        "name": "Charcot-Marie-Tooth disease axonal type 2H",
        "description": "A Charcot-Marie-Tooth disease type 2 that has_material_basis_in variation in the region 8q13-q23."
    },
    "synonyms": [
        {
            "id": "DOID:0110166",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110166",
            "name": "autosomal recessive axonal Charcot-Marie-Tooth disease with pyramidal features",
            "description": ""
        },
        {
            "id": "DOID:0110166",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110166",
            "name": "AR-CMT2C",
            "description": ""
        },
        {
            "id": "DOID:0110166",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110166",
            "name": "Autosomal recessive axonal CMT4C2",
            "description": ""
        },
        {
            "id": "DOID:0110166",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110166",
            "name": "autosomal recessive axonal Charcot-Marie-Tooth neuropathy with pyramidal features",
            "description": ""
        },
        {
            "id": "DOID:0110166",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110166",
            "name": "CMT2H",
            "description": ""
        },
        {
            "id": "DOID:0110166",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110166",
            "name": "Charcot-Marie-Tooth disease type 2H",
            "description": ""
        },
        {
            "id": "DOID:0110166",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110166",
            "name": "Axonal Charcot-Marie-Tooth disease with pyramidal involvement",
            "description": ""
        },
        {
            "id": "MONDO:0011901",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011901",
            "name": "Charcot-Marie-Tooth disease axonal type 2H",
            "description": "Charcot-Marie-Tooth disease, type 2H (CMT2H, also referred to as CMT4C2) is an axonal CMT peripheral sensorimotor polyneuropathy associated with pyramidal involvement."
        },
        {
            "id": "MONDO:0011901",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011901",
            "name": "axonal Charcot-Marie-Tooth disease with pyramidal involvement",
            "description": ""
        },
        {
            "id": "MONDO:0011901",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011901",
            "name": "autosomal recessive axonal Charcot-Marie-Tooth disease with pyramidal features",
            "description": ""
        },
        {
            "id": "MONDO:0011901",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011901",
            "name": "Charcot-Marie-Tooth disease type 2H",
            "description": ""
        },
        {
            "id": "MONDO:0011901",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011901",
            "name": "CMT2H",
            "description": ""
        },
        {
            "id": "MONDO:0011901",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011901",
            "name": "Charcot-Marie-Tooth neuropathy, axonal, with pyramidal features, autosomal recessive",
            "description": ""
        },
        {
            "id": "MONDO:0011901",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011901",
            "name": "Charcot-Marie-Tooth disease, axonal, type 2H",
            "description": ""
        },
        {
            "id": "MONDO:0011901",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011901",
            "name": "AR-CMT2C",
            "description": ""
        },
        {
            "id": "MONDO:0011901",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011901",
            "name": "CMT 2H",
            "description": ""
        },
        {
            "id": "MONDO:0011901",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011901",
            "name": "Charcot Marie Tooth disease type 2H",
            "description": ""
        },
        {
            "id": "MONDO:0011901",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011901",
            "name": "autosomal recessive axonal Charcot-Marie-Tooth neuropathy with pyramidal features",
            "description": ""
        },
        {
            "id": "MONDO:0011901",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011901",
            "name": "autosomal recessive axonal CMT4C2",
            "description": ""
        },
        {
            "id": "MONDO:0011901",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011901",
            "name": "Charcot-Marie-Tooth disease, axonal, with pyramidal features, autosomal recessive",
            "description": ""
        },
        {
            "id": "MONDO:0011901",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011901",
            "name": "Charcot-Marie-Tooth disease, axonal, type 2H; CMT2H",
            "description": ""
        }
    ]
}