{
    "disease_id": "DOID:0110912", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013016", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013016", 
            "name": "leukocyte adhesion deficiency type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013016", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013016", 
            "name": "lad-III"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013016", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013016", 
            "name": "leukocyte adhesion deficiency caused by mutation in FERMT3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013016", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013016", 
            "name": "lad-1 variant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013016", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013016", 
            "name": "IADD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013016", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013016", 
            "name": "leukocyte adhesion deficiency, type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013016", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013016", 
            "name": "leukocyte adhesion deficiency type III"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013016", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013016", 
            "name": "leukocyte adhesion deficiency, type III"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013016", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013016", 
            "name": "LAD1 variant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013016", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013016", 
            "name": "leukocyte adhesion deficiency, type III; LAD3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013016", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013016", 
            "name": "LAD3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013016", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013016", 
            "name": "integrin activation deficiency disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013016", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013016", 
            "name": "leukocyte adhesion deficiency-1 variant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013016", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013016", 
            "name": "FERMT3 leukocyte adhesion deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013016", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013016", 
            "name": "LAD1V"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013016", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013016", 
            "name": "leukocyte adhesion deficiency 1 variant"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110912", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110912", 
            "name": "IADD"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110912", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110912", 
            "name": "LAD1 variant"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110912", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110912", 
            "name": "LAD1V"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110912", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110912", 
            "name": "LAD3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110912", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110912", 
            "name": "integrin activation deficiency disease"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110912", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110912", 
            "name": "leukocyte adhesion deficiency 1 variant"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110912", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110912", 
            "name": "leukocyte adhesion deficiency type III"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110912", 
        "description": "A leukocyte adhesion deficiency that is characterized by a defect in beta integrins 1, 2, and 3; which impairs the integrin activation cascade and has_material_basis_in mutation in FERMT3 gene on chromosome 11q12.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110912", 
        "name": "leukocyte adhesion deficiency 3"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110912#disease-associations", 
            "id": "0110912", 
            "database": "Alliance of Genome Resources"
        }
    ]
}
