{
    "disease_id": "DOID:1206", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013270", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013270", 
            "name": "Rett syndrome, congenital variant"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:1206", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:1206", 
            "name": "Rett's disorder"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:1206", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:1206", 
            "name": "cerebroatrophic hyperammonemia"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:1206", 
        "description": "A pervasive developmental disease that is characterized by normal early growth and development followed by a slowing of development, loss of purposeful use of the hands, distinctive hand movements, slowed brain and head growth, problems with walking, seizures, and intellectual disability.", 
        "resource": "Disease Ontology", 
        "id": "DOID:1206", 
        "name": "Rett syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/1206#disease-associations", 
            "id": "1206", 
            "database": "Alliance of Genome Resources"
        }
    ]
}