{
    "disease_id": "DOID:0110151",
    "recommended_name": {
        "id": "DOID:0110151",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110151",
        "name": "Charcot-Marie-Tooth disease type 1C",
        "description": "A Charcot-Marie-Tooth disease type 1 that has_material_basis_in heterozygous mutation in the LITAF gene on chromosome 16p13."
    },
    "synonyms": [
        {
            "id": "DOID:0110151",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110151",
            "name": "CMT slow nerve conduction type C",
            "description": ""
        },
        {
            "id": "DOID:0110151",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110151",
            "name": "CMT1C",
            "description": ""
        },
        {
            "id": "DOID:0110151",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110151",
            "name": "Charcot-Marie-Tooth neuropathy type 1C",
            "description": ""
        },
        {
            "id": "DOID:0110151",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110151",
            "name": "HMSN IC",
            "description": ""
        },
        {
            "id": "DOID:0110151",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110151",
            "name": "HMSN1C",
            "description": ""
        },
        {
            "id": "DOID:0110151",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110151",
            "name": "neuropathy hereditary motor and sensory type 1C",
            "description": ""
        },
        {
            "id": "MONDO:0010995",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010995",
            "name": "Charcot-Marie-Tooth disease type 1C",
            "description": "Any Charcot-Marie-Tooth disease type 1 in which the cause of the disease is a mutation in the LITAF gene."
        },
        {
            "id": "MONDO:0010995",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010995",
            "name": "CMT1C",
            "description": ""
        },
        {
            "id": "MONDO:0010995",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010995",
            "name": "Charcot-Marie-Tooth disease type 1 caused by mutation in LITAF",
            "description": ""
        },
        {
            "id": "MONDO:0010995",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010995",
            "name": "Charcot-Marie-Tooth disease, type 1C",
            "description": ""
        },
        {
            "id": "MONDO:0010995",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010995",
            "name": "HMSN1C",
            "description": ""
        },
        {
            "id": "MONDO:0010995",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010995",
            "name": "LITAF Charcot-Marie-Tooth disease type 1",
            "description": ""
        },
        {
            "id": "MONDO:0010995",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010995",
            "name": "CMT 1C",
            "description": ""
        },
        {
            "id": "MONDO:0010995",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010995",
            "name": "Charcot Marie Tooth disease type 1C",
            "description": ""
        },
        {
            "id": "MONDO:0010995",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010995",
            "name": "Charcot-Marie-Tooth disease, demyelinating, type 1C",
            "description": ""
        },
        {
            "id": "MIM:601098",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/601098",
            "name": "Charcot-Marie-Tooth disease, demyelinating, type 1C",
            "description": "Charcot-Marie-Tooth disease, demyelinating, type 1C"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110151"
    ],
    "unlinked_id_list": []
}