{
    "disease_id": "DOID:0060769", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011132", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011132", 
            "name": "winged helix deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011132", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011132", 
            "name": "severe T-cell immunodeficiency-congenital alopecia-nail dystrophy syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011132", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011132", 
            "name": "alymphoid cystic thymic dysgenesis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011132", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011132", 
            "name": "T-cell immunodeficiency, congenital alopecia and nail dystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011132", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011132", 
            "name": "alopecia immunodeficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011132", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011132", 
            "name": "congenital alopecia and nail dystrophy associated with severe functional T-cell immunodeficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011132", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011132", 
            "name": "Pignata Guarino syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011132", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011132", 
            "name": "FOXN1 deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060769", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060769", 
            "name": "alymphoid cystic thymic dysgenesis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060769", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060769", 
            "name": "winged helix deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060769", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060769", 
            "name": "severe T-cell immunodeficiency-congenital alopecia-nail dystrophy syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060769", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060769", 
        "name": "T-cell immunodeficiency, congenital alopecia, and nail dystrophy"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060769#disease-associations", 
            "id": "0060769", 
            "database": "Alliance of Genome Resources"
        }
    ]
}