{
    "disease_id": "DOID:0050764",
    "recommended_name": {
        "id": "DOID:0050764",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0050764",
        "name": "Armfield syndrome",
        "description": "A syndromic X-linked intellectual disability characterized by intellectual disability, short stature, seizures, and small hands and feet and in some cases cleft palate or cataracts/glaucoma that has_material_basis_in variation in the chromosomal region Xq28."
    },
    "synonyms": [
        {
            "id": "DOID:0050764",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0050764",
            "name": "Armfield X-linked mental retardation syndrome",
            "description": ""
        },
        {
            "id": "DOID:0050764",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0050764",
            "name": "mental retardation syndrome, X-linked, Armfield type",
            "description": ""
        },
        {
            "id": "DOID:0050764",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0050764",
            "name": "MRXSA",
            "description": ""
        },
        {
            "id": "DOID:0050764",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0050764",
            "name": "X-linked intellectual disability, Armfield type",
            "description": ""
        },
        {
            "id": "DOID:0050764",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0050764",
            "name": "syndromic X-linked mental retardation Armfield type",
            "description": ""
        },
        {
            "id": "MONDO:0010284",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010284",
            "name": "Armfield syndrome",
            "description": "X-linked intellectual disability, Armfield type is characterized by intellectual deficiency, short stature, seizures, and small hands and feet. It has been described in six males from three generations of one family. Three of them also had cataracts/glaucoma and two of them had cleft palate. The locus has been mapped to the terminal 8 Mb of Xq28."
        },
        {
            "id": "MONDO:0010284",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010284",
            "name": "Armfield X-linked intellectual disability syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010284",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010284",
            "name": "Armfield X-linked mental retardation syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010284",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010284",
            "name": "Armfield syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010284",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010284",
            "name": "MRXSA",
            "description": ""
        },
        {
            "id": "MONDO:0010284",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010284",
            "name": "X-linked intellectual disability, Armfield type",
            "description": ""
        },
        {
            "id": "MONDO:0010284",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010284",
            "name": "intellectual developmental disorder, X-linked, syndromic, Armfield type, X-linked recessive",
            "description": ""
        },
        {
            "id": "MONDO:0010284",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010284",
            "name": "intellectual disability syndrome, X-linked, Armfield type",
            "description": ""
        },
        {
            "id": "MONDO:0010284",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010284",
            "name": "mental retardation syndrome, X-linked, armfield type, X-linked recessive",
            "description": ""
        },
        {
            "id": "MONDO:0010284",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010284",
            "name": "syndromic X-linked intellectual disability Armfield type",
            "description": ""
        },
        {
            "id": "MONDO:0010284",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010284",
            "name": "mental retardation, X-linked, syndromic, Armfield type",
            "description": ""
        },
        {
            "id": "MIM:300261",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/300261",
            "name": "Intellectual developmental disorder, X-linked, syndromic, Armfield type",
            "description": "Intellectual developmental disorder, X-linked, syndromic, Armfield type"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0050764"
    ],
    "unlinked_id_list": []
}