{
    "disease_id": "DOID:0080065", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014572", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014572", 
            "name": "Lichtenstein-Knorr syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014572", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014572", 
            "name": "LIKNS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014572", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014572", 
            "name": "progressive autosomal recessive ataxia-deafness syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014572", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014572", 
            "name": "progressive autosomal recessive ataxia-sensorineural hearing loss syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014572", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014572", 
            "name": "SCAR19"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014572", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014572", 
            "name": "Lichtenstein-Knorr syndrome; LIKNS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014572", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014572", 
            "name": "spinocerebellar ataxia, autosomal recessive 19"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014572", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014572", 
            "name": "autosomal recessive spinocerebellar ataxia type 19"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0080065", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080065", 
            "name": "Lichtenstein-Knorr syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080065", 
        "description": "An autosomal recessive cerebellar ataxia that is characterized by postnatal onset of severe progressive sensorineural hearing loss and progressive cerebellar ataxia and that has_material_basis_in homozygous mutation in the SLC9A1 gene on chromosome 1p36.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080065", 
        "name": "autosomal recessive spinocerebellar ataxia 19"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080065#disease-associations", 
            "id": "0080065", 
            "database": "Alliance of Genome Resources"
        }
    ]
}