{
    "disease_id": "DOID:1206", 
    "crossref_internal": {
        "protein": [
            "P51608-1"
        ]
    }, 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010726", 
            "resource": "MONDO", 
            "description": "", 
            "name": "Rett syndrome, atypical", 
            "id": "MONDO:0010726"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010726", 
            "resource": "MONDO", 
            "description": "", 
            "name": "Rett syndrome, preserved speech variant", 
            "id": "MONDO:0010726"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010726", 
            "resource": "MONDO", 
            "description": "", 
            "name": "Rett's disorder", 
            "id": "MONDO:0010726"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010726", 
            "resource": "MONDO", 
            "description": "", 
            "name": "Rts", 
            "id": "MONDO:0010726"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010726", 
            "resource": "MONDO", 
            "description": "", 
            "name": "Rett syndrome; RTT", 
            "id": "MONDO:0010726"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010726", 
            "resource": "MONDO", 
            "description": "", 
            "name": "cerebroatrophic hyperammonemia", 
            "id": "MONDO:0010726"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010726", 
            "resource": "MONDO", 
            "description": "", 
            "name": "RTT", 
            "id": "MONDO:0010726"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010726", 
            "resource": "MONDO", 
            "description": "", 
            "name": "autism, dementia, ataxia, and loss of purposeful hand use", 
            "id": "MONDO:0010726"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010726", 
            "resource": "MONDO", 
            "description": "", 
            "name": "Rett syndrome, Zappella variant", 
            "id": "MONDO:0010726"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:1206", 
            "resource": "Disease Ontology", 
            "description": "", 
            "name": "Rett's disorder", 
            "id": "DOID:1206"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:1206", 
            "resource": "Disease Ontology", 
            "description": "", 
            "name": "cerebroatrophic hyperammonemia", 
            "id": "DOID:1206"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:1206", 
        "resource": "Disease Ontology", 
        "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.", 
        "name": "Rett syndrome", 
        "id": "DOID:1206"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/312750", 
            "id": "312750", 
            "database": "MIM"
        }
    ]
}