{
    "disease_id": "DOID:0080540", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009737", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009737", 
            "name": "neuraminidase/Beta-galactosidase expression"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009737", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009737", 
            "name": "galactosialidosis; GSL"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009737", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009737", 
            "name": "neuraminidase deficiency with beta-galactosidase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009737", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009737", 
            "name": "lysosomal protective Protein deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009737", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009737", 
            "name": "protective Protein/Cathepsin a deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009737", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009737", 
            "name": "cathepsin A deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009737", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009737", 
            "name": "PPCA deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009737", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009737", 
            "name": "GSL"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009737", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009737", 
            "name": "cathepsin A deficiency of"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009737", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009737", 
            "name": "Goldberg syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009737", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009737", 
            "name": "lysosomal protective protein deficiency of"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080540", 
        "description": "A lysosomal storage disease that is characterized by combined deficiency of beta-galactosidase and neuraminidase that has_material_basis_in homozygous or compound heterozygous mutation in the CTSA gene on chromosome 20q13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080540", 
        "name": "galactosialidosis"
    }, 
    "evidence": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009737", 
            "id": "0009737", 
            "database": "MONDO"
        }, 
        {
            "url": "https://www.omim.org/entry/256540", 
            "id": "256540", 
            "database": "MIM"
        }
    ]
}