{
    "disease_id": "DOID:0111043", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013091", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013091", 
            "name": "PHKG2-related glycogen storage disease type IX"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013091", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013091", 
            "name": "GSD9C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013091", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013091", 
            "name": "PHKG2 glycogen storage disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013091", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013091", 
            "name": "GSD type 9C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013091", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013091", 
            "name": "GSD IXc"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013091", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013091", 
            "name": "GSD type IXc"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013091", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013091", 
            "name": "glycogen storage disease type 9C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013091", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013091", 
            "name": "glycogen storage disease type IXc"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013091", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013091", 
            "name": "glycogen storage disease caused by mutation in PHKG2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013091", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013091", 
            "name": "glycogen storage disease IXc; GSD9C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013091", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013091", 
            "name": "glycogenosis type 9C"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111043", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111043", 
            "name": "GSD type 9C"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111043", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111043", 
            "name": "GSD type IXc"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111043", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111043", 
            "name": "GSD9C"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111043", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111043", 
            "name": "glycogen storage disease type 9C"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111043", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111043", 
            "name": "glycogen storage disease type IXc"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111043", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111043", 
            "name": "glycogenosis type 9C"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111043", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111043", 
            "name": "glycogenosis type IXc"
        }, 
        {
            "url": "https://www.omim.org/entry/613027", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:613027", 
            "name": "Glycogen storage disease 9C"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111043", 
        "description": "A glycogen storage disease IX characterized by autosomal recessive inheritance of hepatomegaly, hypotonia, growth retardation, and liver dysfunction with onset in childhood and improvement of symptoms with age that has_material_basis_in homozygous and compound heterozygous mutation in the PHKG2 gene on chromosome 16p11.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111043", 
        "name": "glycogen storage disease IXc"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/613027", 
            "id": "613027", 
            "database": "MIM"
        }
    ]
}