{
    "disease_id": "DOID:0070218", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011153", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011153", 
            "name": "hyperinsulinemic hypoglycemia, familial, 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011153", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011153", 
            "name": "hyperinsulinemic hypoglycemia due to Kir6.2 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011153", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011153", 
            "name": "KCNJ11 hyperinsulinemic hypoglycemia (disease)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011153", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011153", 
            "name": "hyperinsulinemic hypoglycemia (disease) caused by mutation in KCNJ11"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011153", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011153", 
            "name": "hyperinsulinemic hypoglycemia familial 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011153", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011153", 
            "name": "hyperinsulinemic hypoglycemia due to focal adenomatous hyperplasia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011153", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011153", 
            "name": "hyperinsulinism, congenital"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011153", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011153", 
            "name": "hyperinsulinism, neonatal"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011153", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011153", 
            "name": "hyperinsulinemic hypoglycemia, familial, 2; HHF2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011153", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011153", 
            "name": "HHF2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011153", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011153", 
            "name": "hyperinsulinemic hypoglycemia, persistent"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011153", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011153", 
            "name": "hyperinsulinemic hypoglycemia, familial, type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011153", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011153", 
            "name": "Nesidioblastosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011153", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011153", 
            "name": "hyperinsulinism, familial"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011153", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011153", 
            "name": "persistent hyperinsulinemic hypoglycemia of infancy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070218", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070218", 
            "name": "hyperinsulinemic hypoglycemia due to focal adenomatous hyperplasia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070218", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070218", 
            "name": "HHF2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070218", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070218", 
            "name": "Autosomal recessive hyperinsulinemic hypoglycemia due to Kir6.2 deficiency"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070218", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070218", 
        "name": "familial hyperinsulinemic hypoglycemia 2"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0070218#disease-associations", 
            "id": "0070218", 
            "database": "Alliance of Genome Resources"
        }
    ]
}