{
    "disease_id": "DOID:0080765",
    "recommended_name": {
        "id": "DOID:0080765",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0080765",
        "name": "autosomal recessive intellectual developmental disorder-72",
        "description": "A syndromic intellectual disability that has_material_basis_in homozygous mutation in the METTL5 gene on chromosome 2q31."
    },
    "synonyms": [
        {
            "id": "DOID:0080765",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0080765",
            "name": "autosomal recessive mental retardation 72",
            "description": ""
        },
        {
            "id": "MIM:618665",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/618665",
            "name": "Intellectual developmental disorder, autosomal recessive 72",
            "description": "Intellectual developmental disorder, autosomal recessive 72"
        }
    ]
}