{
    "disease_id": "DOID:0070153", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014662", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014662", 
            "name": "congenital insensitivity to pain-hypohidrosis syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014662", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014662", 
            "name": "CIP-hypohidrosis syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014662", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014662", 
            "name": "HSAN8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014662", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014662", 
            "name": "HSAN 8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014662", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014662", 
            "name": "neuropathy, hereditary sensory and autonomic, type VIII"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014662", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014662", 
            "name": "hereditary sensory and autonomic neuropathy type VIII"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014662", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014662", 
            "name": "neuropathy, hereditary sensory and autonomic, type VIII; HSAN8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014662", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014662", 
            "name": "neuropathy, hereditary sensory and autonomic, type 8"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070153", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070153", 
            "name": "hereditary sensory and autonomic neuropathy type VIII"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070153", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070153", 
            "name": "HSAN8"
        }, 
        {
            "url": "https://www.omim.org/entry/616488", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:616488", 
            "name": "Neuropathy, hereditary sensory and autonomic, 8"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070153", 
        "description": "A hereditary sensory neuropathy characterized by congenital insensitivity to pain and decreased sweating and tear production that has_material_basis_in homozygous mutation in the PRDM12 gene on chromosome 9q34.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070153", 
        "name": "hereditary sensory and autonomic neuropathy type 8"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/616488", 
            "id": "616488", 
            "database": "MIM"
        }
    ]
}