{
    "disease_id": "DOID:0070220",
    "recommended_name": {
        "id": "DOID:0070220",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070220",
        "name": "familial hyperinsulinemic hypoglycemia 5",
        "description": "A hyperinsulinemic hypoglycemia characterized by autosomal dominant inheritance of postprandial hypoglycemia, fasting hyperinsulinemia, and an elevated serum insulin-to-C peptide ratio that has_material_basis_in mutation in the INSR gene on chromosome 19p13."
    },
    "synonyms": [
        {
            "id": "DOID:0070220",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070220",
            "name": "hyperinsulinemic hypoglycemia due to INSR deficiency",
            "description": ""
        },
        {
            "id": "DOID:0070220",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070220",
            "name": "HHF5",
            "description": ""
        },
        {
            "id": "DOID:0070220",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070220",
            "name": "hyperinsulinemic hypoglycemia due to insulin receptor deficiency",
            "description": ""
        },
        {
            "id": "DOID:0070220",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070220",
            "name": "hyperinsulinism due to INSR deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0012381",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012381",
            "name": "hyperinsulinism due to INSR deficiency",
            "description": "Hyperinsulinemic hypoglycemia due to INSR deficiency is a very rare autosomal dominant form of familial hyperinsulinism characterized clinically in the single reported family by postprandial hypoglycemia, fasting hyperinsulinemia, and an elevated serum insulin-to-C peptide ratio, and a variable age of onset."
        },
        {
            "id": "MONDO:0012381",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012381",
            "name": "hyperinsulinemic hypoglycemia due to INSR deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0012381",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012381",
            "name": "hyperinsulinemic hypoglycemia due to insulin receptor deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0012381",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012381",
            "name": "hyperinsulinemic hypoglycemia, familial, type 5",
            "description": ""
        },
        {
            "id": "MONDO:0012381",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012381",
            "name": "HHF5",
            "description": ""
        },
        {
            "id": "MONDO:0012381",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012381",
            "name": "hyperinsulinemic hypoglycemia, familial, 5",
            "description": ""
        },
        {
            "id": "MIM:609968",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/609968",
            "name": "Hyperinsulinemic hypoglycemia, familial, 5",
            "description": "Hyperinsulinemic hypoglycemia, familial, 5"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070220"
    ],
    "unlinked_id_list": []
}