{
    "disease_id": "DOID:0060872",
    "recommended_name": {
        "id": "DOID:0060872",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060872",
        "name": "isolated growth hormone deficiency type II",
        "description": "An isolated growth hormone deficiency characterized by autosomal dominant inheritance of low but detectable levels of GH1 resulting in variable degrees of dwarfism which are responsive to growth hormone therapy that has_material_basis_in dominant negative mutations in the GH1 gene on chromosome 17q23.3."
    },
    "synonyms": [
        {
            "id": "DOID:0060872",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060872",
            "name": "IGHD II",
            "description": ""
        },
        {
            "id": "DOID:0060872",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060872",
            "name": "congenital IGHD type II",
            "description": ""
        },
        {
            "id": "DOID:0060872",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060872",
            "name": "congenital isolated GH deficiency type II",
            "description": ""
        },
        {
            "id": "DOID:0060872",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060872",
            "name": "congenital isolated growth hormone deficiency type II",
            "description": ""
        },
        {
            "id": "DOID:0060872",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060872",
            "name": "autosomal dominant isolated growth hormone deficiency",
            "description": ""
        },
        {
            "id": "DOID:0060872",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060872",
            "name": "autosomal dominant pituitary dwarfism due to isolated growth hormone deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0008250",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008250",
            "name": "isolated growth hormone deficiency type II",
            "description": ""
        },
        {
            "id": "MONDO:0008250",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008250",
            "name": "congenital IGHD type II",
            "description": ""
        },
        {
            "id": "MONDO:0008250",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008250",
            "name": "congenital isolated GH deficiency type II",
            "description": ""
        },
        {
            "id": "MONDO:0008250",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008250",
            "name": "congenital isolated growth hormone deficiency type II",
            "description": ""
        },
        {
            "id": "MONDO:0008250",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008250",
            "name": "growth hormone deficiency, isolated, type II",
            "description": ""
        },
        {
            "id": "MONDO:0008250",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008250",
            "name": "Growth hormone deficiency, isolated autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0008250",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008250",
            "name": "IGHD2",
            "description": ""
        },
        {
            "id": "MONDO:0008250",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008250",
            "name": "isolated growth hormone deficiency type 2",
            "description": ""
        },
        {
            "id": "MONDO:0008250",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008250",
            "name": "isolated growth hormone deficiency, type II",
            "description": ""
        },
        {
            "id": "MONDO:0008250",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008250",
            "name": "pituitary dwarfism due to isolated growth hormone deficiency autosomal dominant",
            "description": ""
        },
        {
            "id": "MIM:173100",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/173100",
            "name": "Growth hormone deficiency, isolated, 2",
            "description": "Growth hormone deficiency, isolated, 2"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060872"
    ],
    "unlinked_id_list": []
}