{
    "disease_id": "DOID:0070146",
    "recommended_name": {
        "id": "DOID:0070146",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070146",
        "name": "congenital insensitivity to pain with anhidrosis",
        "description": "A hereditary sensory and autonomic neuropathy characterized by insensitivity to pain and anhidrosis that has_material_basis_in homozygous or compound heterozygous mutation in the NTRK1 gene on chromosome 1q23."
    },
    "synonyms": [
        {
            "id": "DOID:0070146",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070146",
            "name": "hereditary sensory neuropathy type IV",
            "description": ""
        },
        {
            "id": "DOID:0070146",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070146",
            "name": "insensitivity to pain, congenital, with anhidrosis",
            "description": ""
        },
        {
            "id": "DOID:0070146",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070146",
            "name": "hereditary sensory neuropathy type 4",
            "description": ""
        },
        {
            "id": "DOID:0070146",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070146",
            "name": "hereditary sensory and autonomic neuropathy type IV",
            "description": ""
        },
        {
            "id": "DOID:0070146",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070146",
            "name": "CIPA",
            "description": ""
        },
        {
            "id": "DOID:0070146",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070146",
            "name": "HSAN4",
            "description": ""
        },
        {
            "id": "DOID:0070146",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070146",
            "name": "familial dysautonomia type II",
            "description": ""
        },
        {
            "id": "DOID:0070146",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070146",
            "name": "hereditary sensory and autonomic neuropathy type 4",
            "description": ""
        },
        {
            "id": "DOID:0070146",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070146",
            "name": "type II familial dysautonomia",
            "description": ""
        },
        {
            "id": "MONDO:0009746",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009746",
            "name": "hereditary sensory and autonomic neuropathy type 4",
            "description": "Hereditary sensory and autonomic neuropathy, type 4 (HSAN4) is an inherited disorder characterized by anhidrosis, insensitivity to pain, self-mutilating behavior and episodes of fever."
        },
        {
            "id": "MONDO:0009746",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009746",
            "name": "CIP-anhidrosis syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0009746",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009746",
            "name": "HSAN4",
            "description": ""
        },
        {
            "id": "MONDO:0009746",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009746",
            "name": "Hereditary Sensory and Autonomic Neuropathy Type IV",
            "description": ""
        },
        {
            "id": "MONDO:0009746",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009746",
            "name": "NTRK1 hereditary sensory and autonomic neuropathy",
            "description": ""
        },
        {
            "id": "MONDO:0009746",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009746",
            "name": "congenital insensitivity to pain with anhidrosis",
            "description": ""
        },
        {
            "id": "MONDO:0009746",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009746",
            "name": "congenital insensitivity to pain-anhidrosis syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0009746",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009746",
            "name": "hereditary sensory and autonomic neuropathy caused by mutation in NTRK1",
            "description": ""
        },
        {
            "id": "MONDO:0009746",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009746",
            "name": "hereditary sensory and autonomic neuropathy type IV",
            "description": ""
        },
        {
            "id": "MONDO:0009746",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009746",
            "name": "insensitivity to pain, congenital, with anhidrosis",
            "description": ""
        },
        {
            "id": "MONDO:0009746",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009746",
            "name": "CIPA",
            "description": ""
        },
        {
            "id": "MONDO:0009746",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009746",
            "name": "HSAN IV",
            "description": ""
        },
        {
            "id": "MONDO:0009746",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009746",
            "name": "HSNAN4",
            "description": ""
        },
        {
            "id": "MIM:256800",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/256800",
            "name": "Congenital insensitivity to pain with anhidrosis",
            "description": "Congenital insensitivity to pain with anhidrosis"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070146"
    ],
    "unlinked_id_list": []
}