{
    "disease_id": "DOID:0070068", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014617", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014617", 
            "name": "intellectual disability, autosomal dominant 38"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014617", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014617", 
            "name": "EEF1A2 autosomal dominant non-syndromic intellectual disability"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014617", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014617", 
            "name": "mental retardation, autosomal dominant type 38"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014617", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014617", 
            "name": "autosomal dominant mental retardation 38"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014617", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014617", 
            "name": "autosomal dominant non-syndromic intellectual disability caused by mutation in EEF1A2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014617", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014617", 
            "name": "psychomotor retardation, epilepsy, and language disability syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014617", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014617", 
            "name": "PRELDS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014617", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014617", 
            "name": "mental retardation, autosomal dominant 38; MRD38"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014617", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014617", 
            "name": "MRD38"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014617", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014617", 
            "name": "mental retardation, autosomal dominant 38"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070068", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070068", 
            "name": "MRD38"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070068", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070068", 
            "name": "PRELDS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070068", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070068", 
            "name": "autosomal dominant mental retardation 38"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070068", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070068", 
            "name": "psychomotor retardation, epilepsy, and language disability syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070068", 
        "description": "An autosomal dominant non-syndromic intellectual disability that has_material_basis_in an autosomal dominant mutation of EEF1A2 on chromosome 20q13.33.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070068", 
        "name": "autosomal dominant non-syndromic intellectual disability 38"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0070068#disease-associations", 
            "id": "0070068", 
            "database": "Alliance of Genome Resources"
        }
    ]
}