{
    "disease_id": "DOID:0050889", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013624", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013624", 
            "name": "intellectual disability, autosomal recessive 15"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013624", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013624", 
            "name": "mental retardation, autosomal recessive 15"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013624", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013624", 
            "name": "mental retardation, autosomal recessive 15; MRT15"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013624", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013624", 
            "name": "autosomal recessive non-syndromic intellectual disability caused by mutation in MAN1B1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013624", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013624", 
            "name": "mental retardation, autosomal recessive type 15"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013624", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013624", 
            "name": "MAN1B1 autosomal recessive non-syndromic intellectual disability"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013624", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013624", 
            "name": "MRT15"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050889", 
        "description": "An intellectual disability that is characterized by the absence of associated medical and behavioral signs and symptoms.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050889", 
        "name": "non-syndromic intellectual disability"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0050889#disease-associations", 
            "id": "0050889", 
            "database": "Alliance of Genome Resources"
        }
    ]
}