{
    "disease_id": "DOID:0070147", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013634", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013634", 
            "name": "neuropathy, hereditary sensory, type 2C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013634", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013634", 
            "name": "neuropathy, hereditary sensory, type IIC; HSN2C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013634", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013634", 
            "name": "KIF1A hereditary sensory and autonomic neuropathy type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013634", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013634", 
            "name": "neuropathy, hereditary sensory, type IIC"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013634", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013634", 
            "name": "hereditary sensory and autonomic neuropathy type 2 caused by mutation in KIF1A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013634", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013634", 
            "name": "hereditary sensory neuropathy type IIC"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013634", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013634", 
            "name": "HSN2C"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070147", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070147", 
            "name": "HSN2C"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070147", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070147", 
            "name": "hereditary sensory neuropathy type IIC"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070147", 
        "description": "A hereditary sensory and autonomic neuropathy type 2 characterized by peripheral nerve degeneration and progressive distal sensory loss that has_material_basis_in homozygous or compound heterozygous mutation in the KIF1A gene on chromosome 2q37.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070147", 
        "name": "hereditary sensory neuropathy type 2C"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0070147#disease-associations", 
            "id": "0070147", 
            "database": "Alliance of Genome Resources"
        }
    ]
}