{
    "disease_id": "DOID:0060009", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011476", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011476", 
            "name": "bare lymphocyte syndrome type I"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011476", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011476", 
            "name": "immunodeficiency by defective expression of HLA class 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011476", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011476", 
            "name": "Bare lymphocyte syndrome, type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011476", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011476", 
            "name": "HLA Class 1 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011476", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011476", 
            "name": "HLA CLASS I deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011476", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011476", 
            "name": "Bare lymphocyte syndrome type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011476", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011476", 
            "name": "BARE lymphocyte syndrome, type I"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011476", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011476", 
            "name": "BLS type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011476", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011476", 
            "name": "immunodeficiency by defective expression of HLA class type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011476", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011476", 
            "name": "Bls, type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011476", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011476", 
            "name": "BLSI"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011476", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011476", 
            "name": "BLS, type I"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060009", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060009", 
            "name": "BLS, TYPE I"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060009", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060009", 
            "name": "BLSI"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060009", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060009", 
            "name": "HLA CLASS I DEFICIENCY"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060009", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060009", 
            "name": "bare lymphocyte syndrome type I"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060009", 
        "description": "A severe combined immunodeficiency that is characterized by recurrent bacterial, viral, and fungal infections, especially of the lung, and sterile necrotizing granulomas of the skin, develops_from deficiency or decreased surface expression of MHC Class I, has_material_basis_in autosomal recessive inheritance of mutation affecting MHC Class I production or expression and frequently involves TAP1 and TAP2 subunits, and is typically asymptomatic in infancy.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060009", 
        "name": "MHC class I deficiency"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060009#disease-associations", 
            "id": "0060009", 
            "database": "Alliance of Genome Resources"
        }
    ]
}