{
    "disease_id": "DOID:0060874",
    "recommended_name": {
        "id": "DOID:0060874",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060874",
        "name": "isolated growth hormone deficiency type IB",
        "description": "An isolated growth hormone deficiency characterized by autosomal recessive inheritance of low but detectable levels of GH, short stature, significantly retarded bone age, and a positive response and immunologic tolerance to growth hormone therapy that has_material_basis_in mutation in the GH1 or GHRHR genes on chromosomes 17q23.3 and 7p14.3, respectively."
    },
    "synonyms": [
        {
            "id": "DOID:0060874",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060874",
            "name": "IGHD IB",
            "description": ""
        },
        {
            "id": "DOID:0060874",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060874",
            "name": "congenital IGHD type IB",
            "description": ""
        },
        {
            "id": "DOID:0060874",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060874",
            "name": "congenital isolated GH deficiency type IB",
            "description": ""
        },
        {
            "id": "DOID:0060874",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060874",
            "name": "dwarfism of Sindh",
            "description": ""
        },
        {
            "id": "DOID:0060874",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060874",
            "name": "congenital isolated growth hormone deficiency type IB",
            "description": ""
        },
        {
            "id": "MONDO:0013006",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013006",
            "name": "isolated growth hormone deficiency type IB",
            "description": "An isolated growth hormone deficiency characterized by autosomal recessive inheritance of low but detectable levels of GH, short stature, significantly retarded bone age, and a positive response and immunologic tolerance to growth hormone therapy that has material basis in mutation in the GH1 or GHRHR genes on chromosomes 17q23.3 and 7p14.3, respectively."
        },
        {
            "id": "MONDO:0013006",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013006",
            "name": "congenital IGHD type IB",
            "description": ""
        },
        {
            "id": "MONDO:0013006",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013006",
            "name": "congenital isolated GH deficiency type IB",
            "description": ""
        },
        {
            "id": "MONDO:0013006",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013006",
            "name": "congenital isolated growth hormone deficiency type IB",
            "description": ""
        },
        {
            "id": "MONDO:0013006",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013006",
            "name": "dwarfism of Sindh",
            "description": ""
        },
        {
            "id": "MONDO:0013006",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013006",
            "name": "growth hormone deficiency, isolated, type IB",
            "description": ""
        },
        {
            "id": "MONDO:0013006",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013006",
            "name": "IGHD 1B",
            "description": ""
        },
        {
            "id": "MONDO:0013006",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013006",
            "name": "IGHD1B",
            "description": ""
        },
        {
            "id": "MONDO:0013006",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013006",
            "name": "isolated growth hormone deficiency type 1B",
            "description": ""
        },
        {
            "id": "MONDO:0013006",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013006",
            "name": "isolated growth hormone deficiency, type IB",
            "description": ""
        },
        {
            "id": "MONDO:0032567",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032567",
            "name": "isolated growth hormone deficiency, type 4",
            "description": ""
        },
        {
            "id": "MONDO:0032567",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032567",
            "name": "growth hormone deficiency, isolated, type IV",
            "description": ""
        },
        {
            "id": "MONDO:0032567",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032567",
            "name": "IGHD4",
            "description": ""
        },
        {
            "id": "MIM:612781",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/612781",
            "name": "Growth hormone deficiency, isolated, 1B",
            "description": "Growth hormone deficiency, isolated, 1B"
        },
        {
            "id": "MIM:618157",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/618157",
            "name": "Growth hormone deficiency, isolated, 4",
            "description": "Growth hormone deficiency, isolated, 4"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060874"
    ],
    "unlinked_id_list": []
}