{
    "disease_id": "DOID:0070220", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012381", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012381", 
            "name": "hyperinsulinism due to INSR deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012381", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012381", 
            "name": "HHF5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012381", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012381", 
            "name": "hyperinsulinemic hypoglycemia, familial, 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012381", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012381", 
            "name": "hyperinsulinemic hypoglycemia, familial, 5; HHF5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012381", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012381", 
            "name": "hyperinsulinemic hypoglycemia due to insulin receptor deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012381", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012381", 
            "name": "hyperinsulinemic hypoglycemia, familial, type 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012381", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012381", 
            "name": "hyperinsulinemic hypoglycemia due to INSR deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070220", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070220", 
            "name": "hyperinsulinemic hypoglycemia due to INSR deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070220", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070220", 
            "name": "HHF5"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070220", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070220", 
            "name": "hyperinsulinemic hypoglycemia due to insulin receptor deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070220", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070220", 
            "name": "hyperinsulinism due to INSR deficiency"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070220", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070220", 
        "name": "familial hyperinsulinemic hypoglycemia 5"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0070220#disease-associations", 
            "id": "0070220", 
            "database": "Alliance of Genome Resources"
        }
    ]
}