{
    "disease_id": "DOID:0070157", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013337", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013337", 
            "name": "neuropathy, hereditary sensory and autonomic, type 1C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013337", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013337", 
            "name": "HSAN 1C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013337", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013337", 
            "name": "neuropathy, hereditary sensory and autonomic, type IC; HSAN1C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013337", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013337", 
            "name": "neuropathy, hereditary sensory and autonomic, type IC"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013337", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013337", 
            "name": "hereditary sensory and autonomic neuropathy type IC"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013337", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013337", 
            "name": "HSAN1C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013337", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013337", 
            "name": "HSN 1C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013337", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013337", 
            "name": "neuropathy, hereditary sensory, type 1C"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070157", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070157", 
            "name": "HSAN1C"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070157", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070157", 
            "name": "hereditary sensory and autonomic neuropathy type IC"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070157", 
        "description": "A hereditary sensory and autonomic neuropathy type 1 that has_material_basis_in heterozygous mutation in the SPTLC2 gene on chromosome 14q24.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070157", 
        "name": "hereditary sensory and autonomic neuropathy type 1C"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0070157#disease-associations", 
            "id": "0070157", 
            "database": "Alliance of Genome Resources"
        }
    ]
}