{
    "disease_id": "DOID:0060769",
    "recommended_name": {
        "id": "DOID:0060769",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060769",
        "name": "T-cell immunodeficiency, congenital alopecia, and nail dystrophy",
        "description": "A severe combined immunodeficiency characterized by congenital alopecia, severe T-cell immunodeficiency, and ridging, pitting or curving of all nails that has_material_basis_in homozygous mutation in the FOXN1 gene on chromosome 17q11-q12."
    },
    "synonyms": [
        {
            "id": "DOID:0060769",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060769",
            "name": "alymphoid cystic thymic dysgenesis",
            "description": ""
        },
        {
            "id": "DOID:0060769",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060769",
            "name": "winged helix deficiency",
            "description": ""
        },
        {
            "id": "DOID:0060769",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060769",
            "name": "severe T-cell immunodeficiency-congenital alopecia-nail dystrophy syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0011132",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011132",
            "name": "T-cell immunodeficiency, congenital alopecia, and nail dystrophy",
            "description": "A severe combined immunodeficiency characterized by congenital alopecia, severe T-cell immunodeficiency, and ridging, pitting or curving of all nails that has material basis in homozygous mutation in the FOXN1 gene on chromosome 17q11-q12."
        },
        {
            "id": "MONDO:0011132",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011132",
            "name": "FOXN1 deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0011132",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011132",
            "name": "T-cell immunodeficiency, congenital alopecia, and nail dystrophy",
            "description": ""
        },
        {
            "id": "MONDO:0011132",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011132",
            "name": "alopecia immunodeficiency",
            "description": ""
        },
        {
            "id": "MONDO:0011132",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011132",
            "name": "alymphoid cystic thymic dysgenesis",
            "description": ""
        },
        {
            "id": "MONDO:0011132",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011132",
            "name": "severe T-cell immunodeficiency-congenital alopecia-nail dystrophy syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0011132",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011132",
            "name": "winged helix deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0011132",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011132",
            "name": "Pignata Guarino syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0011132",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011132",
            "name": "T-cell immunodeficiency, congenital alopecia and nail dystrophy",
            "description": ""
        },
        {
            "id": "MONDO:0011132",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011132",
            "name": "congenital alopecia and nail dystrophy associated with severe functional T-cell immunodeficiency",
            "description": ""
        },
        {
            "id": "MIM:601705",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/601705",
            "name": "T-cell immunodeficiency, congenital alopecia, and nail dystrophy",
            "description": "T-cell immunodeficiency, congenital alopecia, and nail dystrophy"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060769"
    ],
    "unlinked_id_list": []
}