{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010006", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010006", 
            "name": "Sandhoff disease, infantile type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010006", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010006", 
            "name": "GM2 gangliosidosis, 0 variant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010006", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010006", 
            "name": "GM2 gangliosidosis, type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010006", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010006", 
            "name": "GM2 gangliosidosis 0 variant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010006", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010006", 
            "name": "Sandhoff-Jatzkewitz-Pilz disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010006", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010006", 
            "name": "Hexosaminidases a and B deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010006", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010006", 
            "name": "Sandhoff Jatzkewitz disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010006", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010006", 
            "name": "Beta-hexosaminidase-beta-subunit deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010006", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010006", 
            "name": "Sandhoff disease, juvenile type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010006", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010006", 
            "name": "GM2-gangliosidosis, type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010006", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010006", 
            "name": "total hexosaminidase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010006", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010006", 
            "name": "Sandhoff disease, adult type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010006", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010006", 
            "name": "hexosaminidase A and B deficiency disease"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:3323", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:3323", 
            "name": "Sandhoff Jatzkewitz disease"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:3323", 
        "description": "A GM2 gangliosidosis that is characterized by an accumulation of GM2 gangliosides, particularly in neurons, and that has_material_basis_in mutation in the beta subunit of hexosaminidase (HEXB) on chromosome 5q13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:3323", 
        "name": "Sandhoff disease"
    }, 
    "evidence": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010006", 
            "id": "0010006", 
            "database": "MONDO"
        }, 
        {
            "url": "https://www.omim.org/entry/268800", 
            "id": "268800", 
            "database": "MIM"
        }
    ]
}