{
    "disease_id": "DOID:0110178", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014665", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014665", 
            "name": "hereditary adult-onset painful axonal polyneuropathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014665", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014665", 
            "name": "Charcot-Marie-Tooth disease, axonal, type 2V; CMT2V"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014665", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014665", 
            "name": "autosomal dominant axonal Charcot-Marie-Tooth disease type 2V"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014665", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014665", 
            "name": "CMT2V"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014665", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014665", 
            "name": "NAGLU Charcot-Marie-Tooth disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014665", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014665", 
            "name": "Charcot-Marie-Tooth neuropathy type 2V"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014665", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014665", 
            "name": "Charcot-Marie-Tooth neuropathy, type 2V"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014665", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014665", 
            "name": "Charcot-Marie-Tooth disease caused by mutation in NAGLU"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014665", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014665", 
            "name": "Charcot-Marie-Tooth disease, axonal, type 2V"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014665", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014665", 
            "name": "Charcot-Marie-Tooth disease, axonal, autosomal dominant, type 2V"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014665", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014665", 
            "name": "autosomal dominant Charcot-Marie-Tooth disease type 2V"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014665", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014665", 
            "name": "autosomal dominant Charcot-Marie-Tooth disease type 2 due to NAGLU mutation"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110178", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110178", 
            "name": "autosomal dominant Charcot-Marie-Tooth disease type 2V"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110178", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110178", 
            "name": "CMT2V"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110178", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110178", 
            "name": "Charcot-Marie-Tooth neuropathy type 2V"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110178", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110178", 
            "name": "autosomal dominant axonal Charcot-Marie-Tooth disease type 2V"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110178", 
        "description": "A Charcot-Marie-Tooth disease type 2 that has_material_basis_in heterozygous mutation in the NAGLU gene on chromosome 17q21.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110178", 
        "name": "Charcot-Marie-Tooth disease axonal type 2V"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110178#disease-associations", 
            "id": "0110178", 
            "database": "Alliance of Genome Resources"
        }
    ]
}