{
    "disease_id": "DOID:0070216",
    "recommended_name": {
        "id": "DOID:0070216",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070216",
        "name": "familial hyperinsulinemic hypoglycemia 3",
        "description": "A hyperinsulinemic hypoglycemia characterized by autosomal dominant inheritance of a reduced threshold for insulin release and hypoglycemia induced by fasting or protein rich meals that has_material_basis_in activating mutations in the GCK gene on chromosome 7p13."
    },
    "synonyms": [
        {
            "id": "DOID:0070216",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070216",
            "name": "HHF3",
            "description": ""
        },
        {
            "id": "DOID:0070216",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070216",
            "name": "hyperinsulinism due to glucokinase deficiency",
            "description": ""
        },
        {
            "id": "DOID:0070216",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070216",
            "name": "hyperinsulinemic hypoglycemia due to glucokinase deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0011236",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011236",
            "name": "hyperinsulinemic hypoglycemia, familial, 3",
            "description": "A form of diffuse hyperinsulinism due to glucokinase hyperactivity associated with a variation in the GCK gene, and characterized by an excessive/ uncontrolled insulin secretion (inappropriate for the level of glycemia) and recurrent episodes of hypoglycemia induced by fasting and glucose rich meals."
        },
        {
            "id": "MONDO:0011236",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011236",
            "name": "GCK-related hyperinsulinism",
            "description": ""
        },
        {
            "id": "MONDO:0011236",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011236",
            "name": "HHF3",
            "description": ""
        },
        {
            "id": "MONDO:0011236",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011236",
            "name": "congenital glucokinase-related hyperinsulinism",
            "description": ""
        },
        {
            "id": "MONDO:0011236",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011236",
            "name": "glucokinase-related hyperinsulinemic hypoglycemia",
            "description": ""
        },
        {
            "id": "MONDO:0011236",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011236",
            "name": "hyperinsulinemic hypoglycemia familial 3",
            "description": ""
        },
        {
            "id": "MONDO:0011236",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011236",
            "name": "hyperinsulinemic hypoglycemia, familial, 3",
            "description": ""
        },
        {
            "id": "MONDO:0011236",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011236",
            "name": "hyperinsulinemic hypoglycemia, familial, type 3",
            "description": ""
        },
        {
            "id": "MIM:602485",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/602485",
            "name": "Hyperinsulinemic hypoglycemia, familial, 3",
            "description": "Hyperinsulinemic hypoglycemia, familial, 3"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070216"
    ],
    "unlinked_id_list": []
}