{
    "disease_id": "DOID:0070153",
    "recommended_name": {
        "id": "DOID:0070153",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0070153",
        "name": "hereditary sensory and autonomic neuropathy type 8",
        "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."
    },
    "synonyms": [
        {
            "id": "DOID:0070153",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070153",
            "name": "hereditary sensory and autonomic neuropathy type VIII",
            "description": ""
        },
        {
            "id": "DOID:0070153",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070153",
            "name": "HSAN8",
            "description": ""
        },
        {
            "id": "MONDO:0014662",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014662",
            "name": "congenital insensitivity to pain-hypohidrosis syndrome",
            "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."
        },
        {
            "id": "MONDO:0014662",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014662",
            "name": "CIP-hypohidrosis syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0014662",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014662",
            "name": "HSAN8",
            "description": ""
        },
        {
            "id": "MONDO:0014662",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014662",
            "name": "hereditary sensory and autonomic neuropathy type 8",
            "description": ""
        },
        {
            "id": "MONDO:0014662",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014662",
            "name": "hereditary sensory and autonomic neuropathy type VIII",
            "description": ""
        },
        {
            "id": "MONDO:0014662",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014662",
            "name": "HSAN 8",
            "description": ""
        },
        {
            "id": "MONDO:0014662",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014662",
            "name": "neuropathy, hereditary sensory and autonomic, type 8",
            "description": ""
        },
        {
            "id": "MONDO:0014662",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014662",
            "name": "neuropathy, hereditary sensory and autonomic, type VIII",
            "description": ""
        },
        {
            "id": "MIM:616488",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/616488",
            "name": "Neuropathy, hereditary sensory and autonomic, 8",
            "description": "Neuropathy, hereditary sensory and autonomic, 8"
        }
    ]
}