{
    "disease_id": "DOID:4751", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012205", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012205", 
            "name": "autosomal dominant striatal neurodegeneration type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012205", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012205", 
            "name": "striatal degeneration, autosomal dominant caused by mutation in PDE8B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012205", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012205", 
            "name": "striatal degeneration, autosomal dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012205", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012205", 
            "name": "striatal degeneration, autosomal dominant; ADSD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012205", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012205", 
            "name": "ADSD1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012205", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012205", 
            "name": "striatal degeneration, autosomal dominant 1; ADSD1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012205", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012205", 
            "name": "autosomal dominant striatal neurodegeneration"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012205", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012205", 
            "name": "striatal Degeneration, autosomal dominant 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012205", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012205", 
            "name": "PDE8B striatal degeneration, autosomal dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012205", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012205", 
            "name": "ADSD"
        }, 
        {
            "url": "https://www.omim.org/entry/609161", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:609161", 
            "name": "Striatal degeneration, autosomal dominant 1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:4751", 
        "description": "", 
        "resource": "Disease Ontology", 
        "id": "DOID:4751", 
        "name": "striatonigral degeneration"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/609161", 
            "id": "609161", 
            "database": "MIM"
        }
    ]
}