{
    "disease_id": "DOID:0110198", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014154", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014154", 
            "name": "RI-CMT type C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014154", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014154", 
            "name": "Charcot-Marie-Tooth disease, recessive intermediate C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014154", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014154", 
            "name": "Charcot-Marie-Tooth disease recessive intermediate type C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014154", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014154", 
            "name": "Charcot-Marie-Tooth neuropathy, recessive Intermediate C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014154", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014154", 
            "name": "Charcot-Marie-Tooth disease, recessive intermediate C; CMTRIC"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014154", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014154", 
            "name": "PLEKHG5 Charcot-Marie-Tooth disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014154", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014154", 
            "name": "RI-CMTC"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014154", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014154", 
            "name": "autosomal recessive intermediate Charcot-Marie-Tooth disease type C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014154", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014154", 
            "name": "Charcot-Marie-Tooth disease, recessive Intermediate type C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014154", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014154", 
            "name": "Charcot-Marie-Tooth disease caused by mutation in PLEKHG5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014154", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014154", 
            "name": "CMTRIC"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110198", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110198", 
            "name": "CMTRIC"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110198", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110198", 
            "name": "RI-CMT type C"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110198", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110198", 
            "name": "RI-CMTC"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110198", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110198", 
            "name": "autosomal recessive intermediate Charcot-Marie-Tooth disease type C"
        }, 
        {
            "url": "https://www.omim.org/entry/615376", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:615376", 
            "name": "Charcot-Marie-Tooth disease, recessive, intermediate type, C"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110198", 
        "description": "A Charcot-Marie-Tooth disease intermediate type that has_material_basis_in homozygous or compound heterozygous mutation in the PLEKHG5 gene on chromosome 1p36.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110198", 
        "name": "Charcot-Marie-Tooth disease recessive intermediate C"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/615376", 
            "id": "615376", 
            "database": "MIM"
        }
    ]
}
