{
    "disease_id": "DOID:0111558", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0054833", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0054833", 
            "name": "charcot-marie-tooth disease, axonal, type 2DD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0054833", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0054833", 
            "name": "Charcot-Marie-tooth disease, axonal, type 2DD; CMT2DD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0054833", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0054833", 
            "name": "CMT2DD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0054833", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0054833", 
            "name": "Charcot-Marie-Tooth neuropathy, type 2Dd"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111558", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111558", 
            "name": "ATP1A1-related autosomal dominant Charcot-Marie-Tooth disease type 2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111558", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111558", 
            "name": "ATP1A1-related CMT2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111558", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111558", 
            "name": "CMT2DD"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111558", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111558", 
            "name": "Charcot-Marie-Tooth disease, axonal, type 2DD"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111558", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111558", 
            "name": "Charcot-Marie-Tooth neuropathy, type 2DD"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111558", 
        "description": "A Charcot-Marie-Tooth disease type 2 characterized by neuropathy mainly affecting the lower limbs that has_material_basis_in heterozygous mutation in ATP1A1 on chromosome 1p13.1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111558", 
        "name": "Charcot-Marie-Tooth disease type 2DD"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111558#disease-associations", 
            "id": "0111558", 
            "database": "Alliance of Genome Resources"
        }
    ]
}