{
    "disease_id": "DOID:0110154", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007308", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007308", 
            "name": "Charcot-Marie-Tooth neuropathy type 2A1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007308", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007308", 
            "name": "Charcot-Marie-Tooth disease, axonal, type 2A1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007308", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007308", 
            "name": "hereditary motor and sensory neuropathy IIA1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007308", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007308", 
            "name": "Charcot-Marie-Tooth disease type 2A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007308", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007308", 
            "name": "Charcot-Marie-Tooth disease, neuronal, type 2A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007308", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007308", 
            "name": "Hmsn2A1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007308", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007308", 
            "name": "Charcot-Marie-Tooth disease, axonal, autosomal dominant, type 2A1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007308", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007308", 
            "name": "hereditary motor and sensory neuropathy 2 A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007308", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007308", 
            "name": "CMT2A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007308", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007308", 
            "name": "HMSN IIa1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007308", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007308", 
            "name": "Charcot-Marie-Tooth disease, axonal, type 2A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007308", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007308", 
            "name": "CMT 2A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007308", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007308", 
            "name": "Charcot-Marie-Tooth neuropathy, type 2A1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007308", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007308", 
            "name": "Charcot Marie Tooth disease type 2A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007308", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007308", 
            "name": "CMT2A1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007308", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007308", 
            "name": "Charcot-Marie-Tooth disease neuronal type 2A1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007308", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007308", 
            "name": "autosomal dominant Charcot-Marie-Tooth disease axonal type 2A1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007308", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007308", 
            "name": "KIF1B Charcot-Marie-Tooth disease type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007308", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007308", 
            "name": "autosomal dominant Charcot-Marie-Tooth disease type 2A1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007308", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007308", 
            "name": "HMSN IIA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007308", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007308", 
            "name": "Charcot-Marie-Tooth disease type 2 caused by mutation in KIF1B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007308", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007308", 
            "name": "Charcot-Marie-Tooth disease, axonal, type 2A1; CMT2A1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007308", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007308", 
            "name": "Charcot-Marie-Tooth disease, neuronal, type 2A1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110154", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110154", 
            "name": "CMT2A1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110154", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110154", 
            "name": "Charcot-Marie-Tooth disease neuronal type 2A1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110154", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110154", 
            "name": "Charcot-Marie-Tooth neuropathy type 2A1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110154", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110154", 
            "name": "HMSN IIA1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110154", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110154", 
            "name": "HMSN2A1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110154", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110154", 
            "name": "hereditary motor and sensory neuropathy IIA1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110154", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110154", 
            "name": "autosomal dominant Charcot-Marie-Tooth disease axonal type 2A1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110154", 
        "description": "A Charcot-Marie-Tooth disease type 2 that has_material_basis_in heterozygous mutation in the KIF1B gene on chromosome 1p36.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110154", 
        "name": "Charcot-Marie-Tooth disease type 2A1"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110154#disease-associations", 
            "id": "0110154", 
            "database": "Alliance of Genome Resources"
        }
    ]
}
