{
    "disease_id": "DOID:0070038", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013655", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013655", 
            "name": "intellectual disability, autosomal dominant 8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013655", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013655", 
            "name": "autosomal dominant mental retardation 8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013655", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013655", 
            "name": "MRD8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013655", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013655", 
            "name": "mental retardation, autosomal dominant 8, formerly"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013655", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013655", 
            "name": "NDHMSD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013655", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013655", 
            "name": "GRIN1 autosomal dominant non-syndromic intellectual disability"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013655", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013655", 
            "name": "mental retardation, autosomal dominant 8; MRD8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013655", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013655", 
            "name": "autosomal dominant non-syndromic intellectual disability caused by mutation in GRIN1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013655", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013655", 
            "name": "neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant; NDHMSD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013655", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013655", 
            "name": "neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013655", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013655", 
            "name": "mental retardation, autosomal dominant type 8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013655", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013655", 
            "name": "mental retardation, autosomal dominant 8"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070038", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070038", 
            "name": "MRD8"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070038", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070038", 
            "name": "autosomal dominant mental retardation 8"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070038", 
        "description": "An autosomal dominant non-syndromic intellectual disability that has_material_basis_in an autosomal dominant mutation of GRIN1 on chromosome 9q34.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070038", 
        "name": "autosomal dominant non-syndromic intellectual disability 8"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0070038#disease-associations", 
            "id": "0070038", 
            "database": "Alliance of Genome Resources"
        }
    ]
}