{
    "disease_id": "DOID:0070074",
    "recommended_name": {
        "id": "DOID:0070074",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0070074",
        "name": "autosomal dominant non-syndromic intellectual disability 44",
        "description": "An autosomal dominant non-syndromic intellectual disability that has_material_basis_in an autosomal dominant mutation of TRIO on chromosome 5p15.2."
    },
    "synonyms": [
        {
            "id": "DOID:0070074",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070074",
            "name": "MRD44",
            "description": ""
        },
        {
            "id": "DOID:0070074",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070074",
            "name": "autosomal dominant mental retardation 44",
            "description": ""
        },
        {
            "id": "DOID:0070074",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070074",
            "name": "autosomal dominant intellectual developmental disorder 44 with microcephaly",
            "description": ""
        },
        {
            "id": "MONDO:0014892",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014892",
            "name": "micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0014892",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014892",
            "name": "mercer-Ba syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0014892",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014892",
            "name": "mental retardation, autosomal dominant 44",
            "description": ""
        },
        {
            "id": "MONDO:0014892",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014892",
            "name": "mental retardation, autosomal dominant 44; MRD44",
            "description": ""
        },
        {
            "id": "MONDO:0014892",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014892",
            "name": "MRD44",
            "description": ""
        },
        {
            "id": "MONDO:0014892",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014892",
            "name": "autosomal dominant non-syndromic intellectual disability 44",
            "description": ""
        },
        {
            "id": "MONDO:0014892",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014892",
            "name": "autosomal dominant mental retardation 44",
            "description": ""
        },
        {
            "id": "MONDO:0014892",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014892",
            "name": "MEBAS",
            "description": ""
        },
        {
            "id": "MIM:617061",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/617061",
            "name": "Intellectual developmental disorder, autosomal dominant 44, with microcephaly",
            "description": "Intellectual developmental disorder, autosomal dominant 44, with microcephaly"
        }
    ]
}