{
    "disease_id": "DOID:0070217", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011717", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011717", 
            "name": "hyperinsulinism-hyperammonemia syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011717", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011717", 
            "name": "hyperinsulinism hyperammonemia syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011717", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011717", 
            "name": "hyperinsulinemic hypoglycemia, familial, type 6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011717", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011717", 
            "name": "glutamate dehydrogenase 1 hyperinsulinism"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011717", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011717", 
            "name": "hyperinsulinemic hypoglycemia, familial, 6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011717", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011717", 
            "name": "hi/HA syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011717", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011717", 
            "name": "HHF6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011717", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011717", 
            "name": "HA/hi syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011717", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011717", 
            "name": "hyperinsulinism/hyperammonemia syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011717", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011717", 
            "name": "hyperinsulinemic hypoglycemia, familial, 6; HHF6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011717", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011717", 
            "name": "GLUD1 hyperinsulinism"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011717", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011717", 
            "name": "hyperinsulinemic hypoglycemia familial 6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011717", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011717", 
            "name": "GDH hyperinsulinism"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070217", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070217", 
            "name": "HHF6"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070217", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070217", 
            "name": "HI/HA syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070217", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070217", 
            "name": "hyperinsulinism-hyperammonemia syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070217", 
        "description": "A hyperinsulinemic hypoglycemia characterized by autosomal dominant inheritance of excessive insulin secretion, asymptomatic hyperammonemia and episodes of hypoglycemia induced by fasting or protein rich meals that has_material_basis_in mutation in the GLUD1 gene on chromosome 10q23.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070217", 
        "name": "familial hyperinsulinemic hypoglycemia 6"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/606762", 
            "id": "606762", 
            "database": "MIM"
        }
    ]
}