{
    "disease_id": "DOID:0070218",
    "recommended_name": {
        "id": "DOID:0070218",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070218",
        "name": "familial hyperinsulinemic hypoglycemia 2",
        "description": "A hyperinsulinemic hypoglycemia characterized by autosomal recessive inheritance of severe hyperinsulinemic hypoglycemia that is resistant to diazoxide treatment that has_material_basis_in mutation in the KCNJ11 gene on chromosome 11p15.1."
    },
    "synonyms": [
        {
            "id": "DOID:0070218",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070218",
            "name": "hyperinsulinemic hypoglycemia due to focal adenomatous hyperplasia",
            "description": ""
        },
        {
            "id": "DOID:0070218",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070218",
            "name": "HHF2",
            "description": ""
        },
        {
            "id": "DOID:0070218",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070218",
            "name": "Autosomal recessive hyperinsulinemic hypoglycemia due to Kir6.2 deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0011153",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011153",
            "name": "hyperinsulinemic hypoglycemia, familial, 2",
            "description": "Any hyperinsulinemic hypoglycemia in which the cause of the disease is a mutation in the KCNJ11 gene."
        },
        {
            "id": "MONDO:0011153",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011153",
            "name": "KCNJ11 hyperinsulinemic hypoglycemia (disease)",
            "description": ""
        },
        {
            "id": "MONDO:0011153",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011153",
            "name": "hyperinsulinemic hypoglycemia (disease) caused by mutation in KCNJ11",
            "description": ""
        },
        {
            "id": "MONDO:0011153",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011153",
            "name": "hyperinsulinemic hypoglycemia due to Kir6.2 deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0011153",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011153",
            "name": "hyperinsulinemic hypoglycemia, familial, 2",
            "description": ""
        },
        {
            "id": "MONDO:0011153",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011153",
            "name": "hyperinsulinemic hypoglycemia, familial, type 2",
            "description": ""
        },
        {
            "id": "MONDO:0011153",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011153",
            "name": "HHF2",
            "description": ""
        },
        {
            "id": "MONDO:0011153",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011153",
            "name": "hyperinsulinemic hypoglycemia familial 2",
            "description": ""
        },
        {
            "id": "MIM:601820",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/601820",
            "name": "Hyperinsulinemic hypoglycemia, familial, 2",
            "description": "Hyperinsulinemic hypoglycemia, familial, 2"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070218"
    ],
    "unlinked_id_list": []
}