{
    "disease_id": "DOID:0080473", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0044326", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0044326", 
            "name": "developmental delay and seizures with or without movement abnormalities; DEDSM"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0044326", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0044326", 
            "name": "DEDSM"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080473", 
        "description": "A syndromic intellectual disability characterized by global developmental delay, variable intellectual disability, and early-onset seizures with a myoclonic component that has_material_basis_in heterozygous mutation in the DHDDS gene on chromosome 1p36.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080473", 
        "name": "developmental delay and seizures with or without movement abnormalities"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/617836", 
            "id": "617836", 
            "database": "MIM"
        }
    ]
}