{
    "disease_id": "DOID:0060591", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008674", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008674", 
            "name": "Warts-infections-leukopenia-myelokatexis syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008674", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008674", 
            "name": "Warts, hypogammaglobulinemia, infections, and myelokathexis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008674", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008674", 
            "name": "Warts-hypogammaglobulinemia-infections-myelokathexis syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008674", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008674", 
            "name": "Warts, hypogammaglobulinemia, infections, and myelokathexis syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008674", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008674", 
            "name": "WHIM syndrome; WHIMS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008674", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008674", 
            "name": "WHIMS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008674", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008674", 
            "name": "WILM"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060591", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060591", 
            "name": "WHIMS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060591", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060591", 
            "name": "warts, hypogammaglobulinemia, infections, and myelokathexis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060591", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060591", 
            "name": "warts-hypogammaglobulinemia-infections-myelokathexis syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060591", 
        "description": "An immunodeficiency disease that is characterized by neutropenia, hypogammaglobulinemia, and extensive human papillomavirus infection and that has_material_basis_in heterozygous mutation in the CXCR4 gene on chromosome 2q22.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060591", 
        "name": "WHIM syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060591#disease-associations", 
            "id": "0060591", 
            "database": "Alliance of Genome Resources"
        }
    ]
}