{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014273", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014273", 
            "name": "microcephaly-thin corpus callosum-intellectual disability syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014273", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014273", 
            "name": "mental retardation, autosomal recessive type 40"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014273", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014273", 
            "name": "mental retardation, autosomal recessive 40; MRT40"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014273", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014273", 
            "name": "mental retardation, autosomal recessive 40"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014273", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014273", 
            "name": "MRT40"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060308", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060308", 
            "name": "autosomal recessive non-syndromic mental retardation"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060308", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060308", 
            "name": "autosomal recessive mental retardation"
        }, 
        {
            "url": "https://www.omim.org/entry/615599", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:615599", 
            "name": "Mental retardation, autosomal recessive 40"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060308", 
        "description": "A non-syndromic intellectual disability characterized by an autosomal recessive inheritance pattern.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060308", 
        "name": "autosomal recessive non-syndromic intellectual disability"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/615599", 
            "id": "615599", 
            "database": "MIM"
        }
    ]
}