{
    "disease_id": "DOID:0110192",
    "recommended_name": {
        "id": "DOID:0110192",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110192",
        "name": "Charcot-Marie-Tooth disease type 4H",
        "description": "A Charcot-Marie-Tooth disease type 4 that has_material_basis_in mutations in the gene encoding frabin (FGD4)."
    },
    "synonyms": [
        {
            "id": "DOID:0110192",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110192",
            "name": "autosomal recessive Charcot-Marie-Tooth disease type 4H",
            "description": ""
        },
        {
            "id": "DOID:0110192",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110192",
            "name": "CMT4H",
            "description": ""
        },
        {
            "id": "DOID:0110192",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110192",
            "name": "Charcot-Marie-Tooth neuropathy type 4H",
            "description": ""
        },
        {
            "id": "DOID:0110192",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110192",
            "name": "autosomal recessive demyelinating Charcot-Marie-Tooth disease type 4H",
            "description": ""
        },
        {
            "id": "MONDO:0012250",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012250",
            "name": "Charcot-Marie-Tooth disease type 4H",
            "description": "Charcot-Marie-Tooth disease, type 4H (CMT4H) is a demyelinating CMT peripheral sensorimotor polyneuropathy"
        },
        {
            "id": "MONDO:0012250",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012250",
            "name": "CMT4H",
            "description": ""
        },
        {
            "id": "MONDO:0012250",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012250",
            "name": "Charcot-Marie-Tooth disease type 4 caused by mutation in FGD4",
            "description": ""
        },
        {
            "id": "MONDO:0012250",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012250",
            "name": "Charcot-Marie-Tooth disease type 4H",
            "description": ""
        },
        {
            "id": "MONDO:0012250",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012250",
            "name": "FGD4 Charcot-Marie-Tooth disease type 4",
            "description": ""
        },
        {
            "id": "MONDO:0012250",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012250",
            "name": "Charcot-Marie-Tooth disease, type 4H",
            "description": ""
        },
        {
            "id": "MIM:609311",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/609311",
            "name": "Charcot-Marie-Tooth disease, demyelinating, type 4H",
            "description": "Charcot-Marie-Tooth disease, demyelinating, type 4H"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110192"
    ],
    "unlinked_id_list": []
}