{
    "disease_id": "DOID:0110205", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013758", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013758", 
            "name": "Charcot-Marie-Tooth disease dominant intermediate type E"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013758", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013758", 
            "name": "CMTDIE"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013758", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013758", 
            "name": "Charcot-Marie-Tooth disease, dominant Intermediate type E"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013758", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013758", 
            "name": "Charcot-Marie-Tooth neuropathy with focal segmental glomerulonephritis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013758", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013758", 
            "name": "autosomal dominant intermediate Charcot-Marie-Tooth disease type E"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013758", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013758", 
            "name": "Charcot-Marie-Tooth disease, dominant intermediate E; CMTDIE"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013758", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013758", 
            "name": "Charcot-Marie-Tooth disease, dominant intermediate E"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013758", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013758", 
            "name": "Charcot-Marie-Tooth disease - nephropathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013758", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013758", 
            "name": "Charcot-Marie-Tooth disease-nephropathy syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110205", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110205", 
            "name": "CMTDIE"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110205", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110205", 
            "name": "Charcot-Marie-Tooth disease-nephropathy syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110205", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110205", 
            "name": "Charcot-Marie-Tooth neuropathy with focal segmental glomerulonephritis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110205", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110205", 
            "name": "autosomal dominant intermediate Charcot-Marie-Tooth disease type E"
        }, 
        {
            "url": "https://www.omim.org/entry/614455", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:614455", 
            "name": "Charcot-Marie-Tooth disease, dominant, intermediate type, E"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110205", 
        "description": "A Charcot-Marie-Tooth disease intermediate type that has_material_basis_in heterozygous mutation in the INF2 gene on chromosome 14q32.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110205", 
        "name": "Charcot-Marie-Tooth disease dominant intermediate E"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/614455", 
            "id": "614455", 
            "database": "MIM"
        }
    ]
}