{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008830", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008830", 
            "name": "Aga deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008830", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008830", 
            "name": "AGU"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008830", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008830", 
            "name": "glycosylasparaginase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008830", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008830", 
            "name": "Glycoasparaginase"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008830", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008830", 
            "name": "aspartylglucosaminuria; AGU"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008830", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008830", 
            "name": "aspartylglucosaminidase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008830", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008830", 
            "name": "Aspartylglucosamidase (AGA) deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008830", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008830", 
            "name": "aspartylglycosaminuria"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050461", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050461", 
            "name": "ASPARTYLGLUCOSAMINIDASE DEFICIENCY"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050461", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050461", 
            "name": "GLYCOSYLASPARAGINASE DEFICIENCY"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050461", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050461", 
            "name": "aspartylglycosaminuria"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050461", 
        "description": "A lysosomal storage disease that is characterized by delayed speech at 2-3 years of age, has_material_basis_in mutations in the AGA gene that result in the absence or shortage of the aspartylglucosaminidase enzyme in lysosomes, preventing the normal breakdown of glycoproteins.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050461", 
        "name": "aspartylglucosaminuria"
    }, 
    "evidence": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008830", 
            "id": "0008830", 
            "database": "MONDO"
        }, 
        {
            "url": "https://www.omim.org/entry/208400", 
            "id": "208400", 
            "database": "MIM"
        }
    ]
}