{
    "disease_id": "DOID:0070048", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014034", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014034", 
            "name": "severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014034", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014034", 
            "name": "mental retardation, autosomal dominant type 18"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014034", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014034", 
            "name": "GATAD2B-associated neurodevelopmental disorder"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014034", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014034", 
            "name": "autosomal dominant mental retardation 18"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014034", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014034", 
            "name": "mental retardation, autosomal dominant 18"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014034", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014034", 
            "name": "mental retardation, autosomal dominant 18; MRD18"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014034", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014034", 
            "name": "MRD18"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070048", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070048", 
            "name": "MRD18"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070048", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070048", 
            "name": "autosomal dominant mental retardation 18"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070048", 
        "description": "An autosomal dominant non-syndromic intellectual disability that has_material_basis_in an autosomal dominant mutation of GATAD2B on chromosome 1q21.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070048", 
        "name": "autosomal dominant non-syndromic intellectual disability 18"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0070048#disease-associations", 
            "id": "0070048", 
            "database": "Alliance of Genome Resources"
        }
    ]
}