{
    "disease_id": "DOID:0060875",
    "recommended_name": {
        "id": "DOID:0060875",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0060875",
        "name": "isolated growth hormone deficiency type III",
        "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."
    },
    "synonyms": [
        {
            "id": "DOID:0060875",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060875",
            "name": "Fleisher syndrome",
            "description": ""
        },
        {
            "id": "DOID:0060875",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060875",
            "name": "IGHD III",
            "description": ""
        },
        {
            "id": "DOID:0060875",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060875",
            "name": "congenital isolated growth hormone deficiency type III",
            "description": ""
        },
        {
            "id": "DOID:0060875",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060875",
            "name": "X-linked IGHD",
            "description": ""
        },
        {
            "id": "DOID:0060875",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060875",
            "name": "X-linked isolated growth hormone deficiency",
            "description": ""
        },
        {
            "id": "DOID:0060875",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060875",
            "name": "congenital IGHD type III",
            "description": ""
        },
        {
            "id": "DOID:0060875",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060875",
            "name": "congenital isolated GH deficiency type III",
            "description": ""
        },
        {
            "id": "DOID:0060875",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060875",
            "name": "growth hormone deficiency with hypogammaglobulinemia",
            "description": ""
        },
        {
            "id": "DOID:0060875",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060875",
            "name": "X-linked hypogammaglobulinemia and isolated growth hormone deficiency",
            "description": ""
        },
        {
            "id": "DOID:0060875",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060875",
            "name": "X-linked agammaglobulinemia and isolated growth hormone deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0010615",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010615",
            "name": "isolated growth hormone deficiency type III",
            "description": ""
        },
        {
            "id": "MONDO:0010615",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010615",
            "name": "hypogammaglobulinemia and isolated Growth hormone deficiency, X-linked",
            "description": ""
        },
        {
            "id": "MONDO:0010615",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010615",
            "name": "isolated growth hormone deficiency, type III; IGHD3",
            "description": ""
        },
        {
            "id": "MONDO:0010615",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010615",
            "name": "congenital isolated growth hormone deficiency type III",
            "description": ""
        },
        {
            "id": "MONDO:0010615",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010615",
            "name": "X-linked hypogammaglobulinemia and isolated growth hormone deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0010615",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010615",
            "name": "Growth hormone deficiency with hypogammaglobulinemia",
            "description": ""
        },
        {
            "id": "MONDO:0010615",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010615",
            "name": "IGHD3",
            "description": ""
        },
        {
            "id": "MONDO:0010615",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010615",
            "name": "X-linked agammaglobulinemia and isolated growth hormone deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0010615",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010615",
            "name": "congenital IGHD type III",
            "description": ""
        },
        {
            "id": "MONDO:0010615",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010615",
            "name": "growth hormone deficiency with hypogammaglobulinemia",
            "description": ""
        },
        {
            "id": "MONDO:0010615",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010615",
            "name": "X-linked IGHD",
            "description": ""
        },
        {
            "id": "MONDO:0010615",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010615",
            "name": "IGHD III",
            "description": ""
        },
        {
            "id": "MONDO:0010615",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010615",
            "name": "isolated growth hormone deficiency type 3",
            "description": ""
        },
        {
            "id": "MONDO:0010615",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010615",
            "name": "X-linked isolated growth hormone deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0010615",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010615",
            "name": "IGHD 3",
            "description": ""
        },
        {
            "id": "MONDO:0010615",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010615",
            "name": "Fleisher syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010615",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010615",
            "name": "congenital isolated GH deficiency type III",
            "description": ""
        },
        {
            "id": "MONDO:0010615",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010615",
            "name": "agammaglobulinemia and isolated Growth hormone deficiency, X-linked",
            "description": ""
        },
        {
            "id": "MONDO:0010615",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010615",
            "name": "isolated growth hormone deficiency, type III",
            "description": ""
        },
        {
            "id": "MONDO:0010615",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010615",
            "name": "isolated growth hormone deficiency, type 3",
            "description": ""
        },
        {
            "id": "MIM:307200",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/307200",
            "name": "Growth hormone deficiency, isolated, 3, with agammaglobulinemia",
            "description": "Growth hormone deficiency, isolated, 3, with agammaglobulinemia"
        }
    ]
}