{
    "disease_id": "DOID:0060829",
    "recommended_name": {
        "id": "DOID:0060829",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0060829",
        "name": "obsolete Brooks-Wisniewski-Brown syndrome",
        "description": "A syndromic X-linked intellectual disability characterized by intellectual disability, distinct facial appearance and growth retardation that has_material_basis_in variation on the X chromosome."
    },
    "synonyms": [
        {
            "id": "MONDO:0010376",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010376",
            "name": "Brooks-Wisniewski-brown syndrome",
            "description": "X-linked intellectual disability, Brooks type is a rare X-linked intellectual disability syndrome characterized by failure to thrive, speech delay, intellectual disability, muscle hypotonia, spastic diplegia, optic atrophy with myopia, and distinct facial features (including triangular face, bifrontal narrowness, deeply set eyes, low-set/cupped ears, prominent nose, short philtrum, and thin upper lip with tented morphology) that can be evident from birth. Additional manifestations reported in some patients include large joint contractures and pectus excavatum (which become more evident with age) and seizures."
        },
        {
            "id": "MONDO:0010376",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010376",
            "name": "X-linked mental retardation Brooks type",
            "description": ""
        },
        {
            "id": "MONDO:0010376",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010376",
            "name": "Brooks Wisniewski Brown syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010376",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010376",
            "name": "mental retardation, X-linked, syndromic, Brooks-Wisniewski-Brown type",
            "description": ""
        },
        {
            "id": "MONDO:0010376",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010376",
            "name": "Brooks-Wisniewski-brown syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010376",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010376",
            "name": "X-linked intellectual disability, Brooks type",
            "description": ""
        }
    ]
}