{
    "disease_id": "DOID:0070154",
    "recommended_name": {
        "id": "DOID:0070154",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0070154",
        "name": "hereditary sensory neuropathy type 1F",
        "description": "A hereditary sensory and autonomic neuropathy type 1 characterized by distal sensory impairment becomes apparent during the second or third decade of life, resulting in painless ulceration of the feet with poor healing, which can progress to osteomyelitis, bone destruction, and amputation that has_material_basis_in heterozygous mutation in the ATL3 gene on chromosome 11q13."
    },
    "synonyms": [
        {
            "id": "DOID:0070154",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070154",
            "name": "HSN1F",
            "description": ""
        },
        {
            "id": "DOID:0070154",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070154",
            "name": "hereditary sensory neuropathy type IF",
            "description": ""
        },
        {
            "id": "MONDO:0014286",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014286",
            "name": "neuropathy, hereditary sensory, type 1F",
            "description": "Any hereditary sensory and autonomic neuropathy type 1 in which the cause of the disease is a mutation in the ATL3 gene."
        },
        {
            "id": "MONDO:0014286",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014286",
            "name": "HSN 1F",
            "description": ""
        },
        {
            "id": "MONDO:0014286",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014286",
            "name": "HSN1F",
            "description": ""
        },
        {
            "id": "MONDO:0014286",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014286",
            "name": "hereditary sensory and autonomic neuropathy type 1 caused by mutation in ATL3",
            "description": ""
        },
        {
            "id": "MONDO:0014286",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014286",
            "name": "ATL3 hereditary sensory and autonomic neuropathy type 1",
            "description": ""
        },
        {
            "id": "MONDO:0014286",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014286",
            "name": "hereditary sensory neuropathy type 1F",
            "description": ""
        },
        {
            "id": "MONDO:0014286",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014286",
            "name": "neuropathy, hereditary sensory, type IF; HSN1F",
            "description": ""
        },
        {
            "id": "MONDO:0014286",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014286",
            "name": "hereditary sensory neuropathy type IF",
            "description": ""
        },
        {
            "id": "MONDO:0014286",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014286",
            "name": "neuropathy, hereditary sensory, type IF",
            "description": ""
        },
        {
            "id": "MIM:615632",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/615632",
            "name": "Neuropathy, hereditary sensory, 1F",
            "description": "Neuropathy, hereditary sensory, 1F"
        }
    ]
}