{
    "disease_id": "DOID:0090103",
    "recommended_name": {
        "id": "DOID:0090103",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0090103",
        "name": "Huntington's disease-like 1",
        "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."
    },
    "synonyms": [
        {
            "id": "DOID:0090103",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0090103",
            "name": "HDL1",
            "description": ""
        },
        {
            "id": "DOID:0090103",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0090103",
            "name": "HLN1",
            "description": ""
        },
        {
            "id": "DOID:0090103",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0090103",
            "name": "Huntington disease-like 1",
            "description": ""
        },
        {
            "id": "DOID:0090103",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0090103",
            "name": "Huntington-like neurodegenerative disorder 1",
            "description": ""
        },
        {
            "id": "DOID:0090103",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0090103",
            "name": "autosomal dominant Huntington-like neurodegenerative disorder",
            "description": ""
        },
        {
            "id": "DOID:0090103",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0090103",
            "name": "early-onset prion disease with prominent psychiatric features",
            "description": ""
        },
        {
            "id": "MONDO:0011299",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011299",
            "name": "Huntington disease-like 1",
            "description": "Any neurodegenerative disease with chorea in which the cause of the disease is a mutation in the PRNP gene."
        },
        {
            "id": "MONDO:0011299",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011299",
            "name": "HDL1",
            "description": ""
        },
        {
            "id": "MONDO:0011299",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011299",
            "name": "Huntington disease-like 1",
            "description": ""
        },
        {
            "id": "MONDO:0011299",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011299",
            "name": "Huntington-like neurodegenerative disorder, autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0011299",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011299",
            "name": "Huntington disease-like type 1",
            "description": ""
        },
        {
            "id": "MONDO:0011299",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011299",
            "name": "Huntington-like neurodegenerative disorder 1",
            "description": ""
        },
        {
            "id": "MONDO:0011299",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011299",
            "name": "prion disease, early-onset, with prominent psychiatric features",
            "description": ""
        },
        {
            "id": "MONDO:0011299",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011299",
            "name": "autosomal dominant Huntington-like neurodegenerative disorder",
            "description": ""
        },
        {
            "id": "MONDO:0011299",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011299",
            "name": "Huntington disease-like 1; HDL1",
            "description": ""
        },
        {
            "id": "MONDO:0011299",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011299",
            "name": "HLN1",
            "description": ""
        },
        {
            "id": "MONDO:0011299",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011299",
            "name": "early-onset prion disease with prominent psychiatric features",
            "description": ""
        },
        {
            "id": "MONDO:0011299",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011299",
            "name": "PRNP neurodegenerative disease with chorea",
            "description": ""
        },
        {
            "id": "MONDO:0011299",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011299",
            "name": "neurodegenerative disease with chorea caused by mutation in PRNP",
            "description": ""
        },
        {
            "id": "MONDO:0011299",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011299",
            "name": "Huntington's disease-like 1",
            "description": ""
        },
        {
            "id": "MIM:603218",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/603218",
            "name": "Huntington disease-like 1",
            "description": "Huntington disease-like 1"
        }
    ]
}