{
    "disease_id": "DOID:0112060",
    "recommended_name": {
        "id": "DOID:0112060",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0112060",
        "name": "Raynaud-Claes syndrome",
        "description": "A syndromic X-linked intellectual disability characterized by borderline to severe intellectual disability, impaired language development, and variable additional features including; behavioral problems, psychiatric disorders, seizures, progressive ataxia, brain abnormalities, and facial dysmorphisms that has_material_basis_in heterozygous or hemizygous mutation in the CLCN4 gene on chromosome Xp22.2."
    },
    "synonyms": [
        {
            "id": "DOID:0112060",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0112060",
            "name": "MRX15",
            "description": ""
        },
        {
            "id": "DOID:0112060",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0112060",
            "name": "MRX49",
            "description": ""
        },
        {
            "id": "DOID:0112060",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0112060",
            "name": "MRXSRC",
            "description": ""
        },
        {
            "id": "DOID:0112060",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0112060",
            "name": "X-linked mental retardation 15",
            "description": ""
        },
        {
            "id": "DOID:0112060",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0112060",
            "name": "X-linked mental retardation 49",
            "description": ""
        },
        {
            "id": "MONDO:0010250",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010250",
            "name": "intellectual disability, X-linked 49",
            "description": ""
        },
        {
            "id": "MONDO:0010250",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010250",
            "name": "CLCN4-related X-linked intellectual disability syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010250",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010250",
            "name": "MRX49",
            "description": ""
        },
        {
            "id": "MONDO:0010250",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010250",
            "name": "Raynaud-Claes syndrome, X-linked dominant",
            "description": ""
        },
        {
            "id": "MONDO:0010250",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010250",
            "name": "intellectual disability, X-linked 15",
            "description": ""
        },
        {
            "id": "MONDO:0010250",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010250",
            "name": "intellectual disability, X-linked 49",
            "description": ""
        },
        {
            "id": "MONDO:0010250",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010250",
            "name": "mental retardation, X-linked 15",
            "description": ""
        },
        {
            "id": "MONDO:0010250",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010250",
            "name": "mental retardation, X-linked 49",
            "description": ""
        },
        {
            "id": "MIM:300114",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/300114",
            "name": "Raynaud-Claes syndrome",
            "description": "Raynaud-Claes syndrome"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0112060"
    ],
    "unlinked_id_list": []
}