{
    "disease_id": "DOID:12858", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:12858", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:12858", 
            "name": "Huntington disease"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:12858", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:12858", 
            "name": "Huntington's chorea"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:12858", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:12858", 
            "name": "HD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007739", 
            "description": "Huntington disease (HD) is a rare neurodegenerative disorder of the central nervous system characterized by unwanted choreatic movements, behavioral and psychiatric disturbances and dementia.", 
            "resource": "MONDO", 
            "id": "MONDO:0007739", 
            "name": "Huntington disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007739", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007739", 
            "name": "Huntington's chorea"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007739", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007739", 
            "name": "Huntington's disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007739", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007739", 
            "name": "Huntington disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007739", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007739", 
            "name": "Huntington disease; HD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007739", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007739", 
            "name": "Huntington chorea"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007739", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007739", 
            "name": "HD"
        }, 
        {
            "url": "https://www.omim.org/entry/143100", 
            "description": "Huntington disease", 
            "resource": "MIM", 
            "id": "MIM:143100", 
            "name": "Huntington disease"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:12858", 
        "description": "A neurodegenerative disease that has_material_basis_in autosomal dominant inheritance and is characterized by unwanted choreatic movements, behavioral and psychiatric disturbances and dementia and has_material_basis_in expansion of CAG triplet repeats (glutamine) resulting in neuron degeneration affecting muscle coordination, cognitive abilities.", 
        "resource": "Disease Ontology", 
        "id": "DOID:12858", 
        "name": "Huntington's disease"
    }
}