{
    "disease_id": "DOID:0070156", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013381", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013381", 
            "name": "neuropathy, hereditary sensory, type 1D"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013381", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013381", 
            "name": "neuropathy, hereditary sensory, type ID; HSN1D"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013381", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013381", 
            "name": "neuropathy, hereditary sensory, type ID"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013381", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013381", 
            "name": "HSN1D"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013381", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013381", 
            "name": "hereditary sensory neuropathy type ID"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070156", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070156", 
            "name": "HSN1D"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070156", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070156", 
        "name": "hereditary sensory neuropathy type 1D"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0070156#disease-associations", 
            "id": "0070156", 
            "database": "Alliance of Genome Resources"
        }
    ]
}