{
    "disease_id": "DOID:0070156",
    "recommended_name": {
        "id": "DOID:0070156",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0070156",
        "name": "hereditary sensory neuropathy type 1D",
        "description": "A hereditary sensory and autonomic neuropathy type 1 characterized dult onset of a distal axonal sensory neuropathy affecting all modalities, often associated with distal ulceration and amputation as well as hyporeflexia, although some patients may show features suggesting upper neuron involvement that has_material_basis_in heterozygous mutation in the ATL1 gene on chromosome 14q."
    },
    "synonyms": [
        {
            "id": "DOID:0070156",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070156",
            "name": "HSN1D",
            "description": ""
        },
        {
            "id": "MONDO:0013381",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013381",
            "name": "neuropathy, hereditary sensory, type 1D",
            "description": "A hereditary sensory and autonomic neuropathy type 1 characterized by adult onset of a distal axonal sensory neuropathy that has material basis in heterozygous mutation in the ATL1 gene on chromosome 14q."
        },
        {
            "id": "MONDO:0013381",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013381",
            "name": "HSN1D",
            "description": ""
        },
        {
            "id": "MONDO:0013381",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013381",
            "name": "hereditary sensory neuropathy type 1D",
            "description": ""
        },
        {
            "id": "MONDO:0013381",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013381",
            "name": "hereditary sensory neuropathy type ID",
            "description": ""
        },
        {
            "id": "MONDO:0013381",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013381",
            "name": "neuropathy, hereditary sensory, type ID",
            "description": ""
        },
        {
            "id": "MIM:613708",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/613708",
            "name": "Neuropathy, hereditary sensory, 1D",
            "description": "Neuropathy, hereditary sensory, 1D"
        }
    ]
}