{
    "disease_id": "DOID:0090103", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011299", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011299", 
            "name": "Huntington disease-like 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011299", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011299", 
            "name": "HDL1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011299", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011299", 
            "name": "Huntington-like neurodegenerative disorder, autosomal dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011299", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011299", 
            "name": "Huntington disease-like type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011299", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011299", 
            "name": "Huntington-like neurodegenerative disorder 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011299", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011299", 
            "name": "prion disease, early-onset, with prominent psychiatric features"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011299", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011299", 
            "name": "autosomal dominant Huntington-like neurodegenerative disorder"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011299", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011299", 
            "name": "Huntington disease-like 1; HDL1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011299", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011299", 
            "name": "HLN1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011299", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011299", 
            "name": "early-onset prion disease with prominent psychiatric features"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011299", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011299", 
            "name": "PRNP neurodegenerative disease with chorea"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011299", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011299", 
            "name": "neurodegenerative disease with chorea caused by mutation in PRNP"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090103", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090103", 
            "name": "HDL1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090103", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090103", 
            "name": "HLN1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090103", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090103", 
            "name": "Huntington disease-like 1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090103", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090103", 
            "name": "Huntington-like neurodegenerative disorder 1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090103", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090103", 
            "name": "autosomal dominant Huntington-like neurodegenerative disorder"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090103", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090103", 
            "name": "early-onset prion disease with prominent psychiatric features"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0090103", 
        "description": "A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0090103", 
        "name": "Huntington's disease-like 1"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0090103#disease-associations", 
            "id": "0090103", 
            "database": "Alliance of Genome Resources"
        }
    ]
}