{
    "disease_id": "DOID:0112020",
    "recommended_name": {
        "id": "DOID:0112020",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0112020",
        "name": "non-syndromic X-linked intellectual disability 103",
        "description": "A non-syndromic X-linked intellectual disability characterized by intellectual disability and facial feature anomalies that has_material_basis_in hemizygous mutation in the KLHL15 gene on chromosome Xp22.11."
    },
    "synonyms": [
        {
            "id": "DOID:0112020",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112020",
            "name": "MRX103",
            "description": ""
        },
        {
            "id": "DOID:0112020",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112020",
            "name": "X-linked mental retardation 103",
            "description": ""
        },
        {
            "id": "MONDO:0010508",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010508",
            "name": "intellectual disability, X-linked 103",
            "description": "Any non-syndromic X-linked intellectual disability in which the cause of the disease is a mutation in the KLHL15 gene."
        },
        {
            "id": "MONDO:0010508",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010508",
            "name": "KLHL15 non-syndromic X-linked intellectual disability",
            "description": ""
        },
        {
            "id": "MONDO:0010508",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010508",
            "name": "MRX103",
            "description": ""
        },
        {
            "id": "MONDO:0010508",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010508",
            "name": "intellectual developmental disorder, X-linked 103, X-linked recessive",
            "description": ""
        },
        {
            "id": "MONDO:0010508",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010508",
            "name": "intellectual disability, X-linked 103",
            "description": ""
        },
        {
            "id": "MONDO:0010508",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010508",
            "name": "intellectual disability, X-linked type 103",
            "description": ""
        },
        {
            "id": "MONDO:0010508",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010508",
            "name": "mental retardation, X-linked 103",
            "description": ""
        },
        {
            "id": "MONDO:0010508",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010508",
            "name": "mental retardation, X-linked type 103",
            "description": ""
        },
        {
            "id": "MONDO:0010508",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010508",
            "name": "non-syndromic X-linked intellectual disability caused by mutation in KLHL15",
            "description": ""
        },
        {
            "id": "MIM:300982",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/300982",
            "name": "Intellectual developmental disorder, X-linked 103",
            "description": "Intellectual developmental disorder, X-linked 103"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0112020"
    ],
    "unlinked_id_list": []
}