{
    "disease_id": "DOID:0110151", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010995", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010995", 
            "name": "Charcot-Marie-Tooth neuropathy, type 1C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010995", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010995", 
            "name": "HMSN IC"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010995", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010995", 
            "name": "CMT slow nerve conduction type C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010995", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010995", 
            "name": "neuropathy, hereditary motor and sensory, type 1C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010995", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010995", 
            "name": "HMSN 1C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010995", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010995", 
            "name": "CMT 1C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010995", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010995", 
            "name": "Charcot Marie Tooth disease type 1C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010995", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010995", 
            "name": "CMT, slow nerve conduction type C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010995", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010995", 
            "name": "Charcot-Marie-Tooth neuropathy type 1C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010995", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010995", 
            "name": "Charcot-Marie-Tooth disease, demyelinating, type 1C; CMT1C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010995", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010995", 
            "name": "neuropathy hereditary motor and sensory type 1C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010995", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010995", 
            "name": "HMSN1C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010995", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010995", 
            "name": "Charcot-Marie-Tooth disease type 1 caused by mutation in LITAF"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010995", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010995", 
            "name": "CMT1C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010995", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010995", 
            "name": "Charcot-Marie-Tooth disease, demyelinating, type 1C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010995", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010995", 
            "name": "LITAF Charcot-Marie-Tooth disease type 1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110151", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110151", 
            "name": "CMT slow nerve conduction type C"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110151", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110151", 
            "name": "CMT1C"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110151", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110151", 
            "name": "Charcot-Marie-Tooth neuropathy type 1C"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110151", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110151", 
            "name": "HMSN IC"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110151", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110151", 
            "name": "HMSN1C"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110151", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110151", 
            "name": "neuropathy hereditary motor and sensory type 1C"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110151", 
        "description": "A Charcot-Marie-Tooth disease type 1 that has_material_basis_in heterozygous mutation in the LITAF gene on chromosome 16p13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110151", 
        "name": "Charcot-Marie-Tooth disease type 1C"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110151#disease-associations", 
            "id": "0110151", 
            "database": "Alliance of Genome Resources"
        }
    ]
}
