{
    "disease_id": "DOID:0050629", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012429", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012429", 
            "name": "Aicardi-Goutieres syndrome 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012429", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012429", 
            "name": "Aicardi-Goutieres syndrome type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012429", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012429", 
            "name": "AGS2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012429", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012429", 
            "name": "Aicardi-Goutieres syndrome 2; AGS2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012429", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012429", 
            "name": "RNASEH2B Aicardi-Goutieres syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012429", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012429", 
            "name": "Aicardi-Goutieres syndrome caused by mutation in RNASEH2B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012429", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012429", 
            "name": "RNASEH2B-related Aicardi-Goutieres syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050629", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050629", 
            "name": "Cree encephalitis"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050629", 
        "description": "A syndrome that is a genetically heterogeneous encephalopathy characterized in its most severe form by cerebral atrophy, leukodystrophy, intracranial calcifications, chronic cerebrospinal fluid lymphocytosis, increased CSF alpha-interferon, and negative serologic investigations for common prenatal infections.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050629", 
        "name": "Aicardi-Goutieres syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0050629#disease-associations", 
            "id": "0050629", 
            "database": "Alliance of Genome Resources"
        }
    ]
}