{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012946", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012946", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012946", 
            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012946", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012946", 
            "name": "autosomal dominant non-syndromic intellectual disability caused by mutation in CDH15"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012946", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012946", 
            "name": "mental retardation, autosomal dominant 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012946", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012946", 
            "name": "mental retardation, autosomal dominant 3; MRD3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012946", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012946", 
            "name": "CDH15 autosomal dominant non-syndromic intellectual disability"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012946", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012946", 
            "name": "MRD3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012946", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012946", 
            "name": "autosomal dominant mental retardation 3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070033", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070033", 
            "name": "MRD3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070033", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070033", 
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        }, 
        {
            "url": "https://www.omim.org/entry/612580", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:612580", 
            "name": "Mental retardation, autosomal dominant 3"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070033", 
        "description": "An autosomal dominant non-syndromic intellectual disability that has_material_basis_in an autosomal dominant mutation of CDH15 on chromosome 16q24.3.", 
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        "name": "autosomal dominant non-syndromic intellectual disability 3"
    }, 
    "evidence": [
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            "url": "https://www.omim.org/entry/612580", 
            "id": "612580", 
            "database": "MIM"
        }
    ]
}