{
    "disease_id": "DOID:0070145",
    "recommended_name": {
        "id": "DOID:0070145",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070145",
        "name": "hereditary sensory and autonomic neuropathy type 5",
        "description": "A hereditary sensory and autonomic neuropathy characterized by impaired pain and thermal perception in the extremities and selective reduction in small myelinated fibers that has_material_basis_in homozygous mutation in the NGF gene on chromosome 1p13."
    },
    "synonyms": [
        {
            "id": "DOID:0070145",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070145",
            "name": "HSAN5",
            "description": ""
        },
        {
            "id": "DOID:0070145",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070145",
            "name": "hereditary sensory and autonomic neuropathy type V",
            "description": ""
        },
        {
            "id": "MONDO:0012092",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012092",
            "name": "hereditary sensory and autonomic neuropathy type 5",
            "description": "Hereditary sensory and autonomic neuropathy, type 5 (HSAN5) is characterized by loss of pain perception and impaired temperature sensitivity, in the absence of any other major neurological anomalies."
        },
        {
            "id": "MONDO:0012092",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012092",
            "name": "HSAN5",
            "description": ""
        },
        {
            "id": "MONDO:0012092",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012092",
            "name": "NGF autosomal recessive hereditary sensory and autonomic neuropathy",
            "description": ""
        },
        {
            "id": "MONDO:0012092",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012092",
            "name": "autosomal recessive hereditary sensory and autonomic neuropathy caused by mutation in NGF",
            "description": ""
        },
        {
            "id": "MONDO:0012092",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012092",
            "name": "congenital insensitivity to pain and thermal analgesia",
            "description": ""
        },
        {
            "id": "MONDO:0012092",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012092",
            "name": "hereditary sensory and autonomic neuropathy type V",
            "description": ""
        },
        {
            "id": "MONDO:0012092",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012092",
            "name": "HSAN V",
            "description": ""
        },
        {
            "id": "MONDO:0012092",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012092",
            "name": "neuropathy, hereditary sensory and autonomic, type V",
            "description": ""
        },
        {
            "id": "MIM:608654",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/608654",
            "name": "Neuropathy, hereditary sensory and autonomic, 5",
            "description": "Neuropathy, hereditary sensory and autonomic, 5"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070145"
    ],
    "unlinked_id_list": []
}