{
    "disease_id": "DOID:0060875", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010615", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010615", 
            "name": "hypogammaglobulinemia and isolated Growth hormone deficiency, X-linked"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010615", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010615", 
            "name": "isolated growth hormone deficiency, type III; IGHD3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010615", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010615", 
            "name": "congenital isolated growth hormone deficiency type III"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010615", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010615", 
            "name": "X-linked hypogammaglobulinemia and isolated growth hormone deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010615", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010615", 
            "name": "Growth hormone deficiency with hypogammaglobulinemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010615", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010615", 
            "name": "IGHD3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010615", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010615", 
            "name": "X-linked agammaglobulinemia and isolated growth hormone deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010615", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010615", 
            "name": "congenital IGHD type III"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010615", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010615", 
            "name": "X-linked IGHD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010615", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010615", 
            "name": "IGHD III"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010615", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010615", 
            "name": "isolated growth hormone deficiency type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010615", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010615", 
            "name": "X-linked isolated growth hormone deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010615", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010615", 
            "name": "IGHD 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010615", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010615", 
            "name": "Fleisher syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010615", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010615", 
            "name": "congenital isolated GH deficiency type III"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010615", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010615", 
            "name": "agammaglobulinemia and isolated Growth hormone deficiency, X-linked"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010615", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010615", 
            "name": "isolated growth hormone deficiency, type III"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010615", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010615", 
            "name": "isolated growth hormone deficiency, type 3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060875", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060875", 
            "name": "Fleisher syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060875", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060875", 
            "name": "IGHD III"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060875", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060875", 
            "name": "congenital isolated growth hormone deficiency type III"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060875", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060875", 
            "name": "X-linked IGHD"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060875", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060875", 
            "name": "X-linked isolated growth hormone deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060875", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060875", 
            "name": "congenital IGHD type III"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060875", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060875", 
            "name": "congenital isolated GH deficiency type III"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060875", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060875", 
            "name": "growth hormone deficiency with hypogammaglobulinemia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060875", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060875", 
            "name": "X-linked hypogammaglobulinemia and isolated growth hormone deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060875", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060875", 
            "name": "X-linked agammaglobulinemia and isolated growth hormone deficiency"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060875", 
        "description": "An isolated growth hormone deficiency characterized by dwarfism, variable occurence of hypogammaglobulinemia, and a generally good response to growth hormone therapy that has material_basis_in mutation in the BTK gene on chromosome Xq22.1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060875", 
        "name": "isolated growth hormone deficiency type III"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060875#disease-associations", 
            "id": "0060875", 
            "database": "Alliance of Genome Resources"
        }
    ]
}