{
    "disease_id": "DOID:0070158", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013584", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013584", 
            "name": "hereditary sensory neuropathy-deafness-dementia syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013584", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013584", 
            "name": "hereditary sensory neuropathy-sensorineural hearing loss-dementia syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013584", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013584", 
            "name": "hereditary sensory neuropathy with hearing loss and dementia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013584", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013584", 
            "name": "neuropathy, hereditary sensory, type IE; HSN1E"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013584", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013584", 
            "name": "hereditary sensory neuropathy type IE"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013584", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013584", 
            "name": "DNMT1-related dementia, deafness, and sensory neuropathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013584", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013584", 
            "name": "HSNIE"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013584", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013584", 
            "name": "neuropathy, hereditary sensory, type IE"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013584", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013584", 
            "name": "hereditary sensory and autonomic neuropathy type 1E"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013584", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013584", 
            "name": "neuropathy, hereditary sensory, type 1E"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013584", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013584", 
            "name": "HSN 1E"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013584", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013584", 
            "name": "HSN1E"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013584", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013584", 
            "name": "neuropathy, hereditary sensory, with hearing loss and dementia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013584", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013584", 
            "name": "HSAN1E"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070158", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070158", 
            "name": "HSN1E"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070158", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070158", 
            "name": "hereditary sensory neuropathy type IE"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070158", 
        "description": "A hereditary sensory neuropathy characterized by adult onset of progressive peripheral sensory loss, progressive hearing impairment, and early-onset dementia that has_material_basis_in heterozygous mutation in the DNMT1 gene on chromosome 19p13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070158", 
        "name": "hereditary sensory neuropathy type 1E"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0070158#disease-associations", 
            "id": "0070158", 
            "database": "Alliance of Genome Resources"
        }
    ]
}