{
    "disease_id": "DOID:3320", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010100", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010100", 
            "name": "hexosaminidase a deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010100", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010100", 
            "name": "TSD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010100", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010100", 
            "name": "Tay-Sachs disease, juvenile"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010100", 
            "name": "GM2-gangliosidosis, type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010100", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010100", 
            "name": "GM2 gangliosidosis, type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010100", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010100", 
            "name": "GM2-gangliosidosis, variant B1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010100", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010100", 
            "name": "GM2-gangliosidosis, adult chronic type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010100", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010100", 
            "name": "Tay-Sachs disease, variant B1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010100", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010100", 
            "name": "B variant GM2 gangliosidosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010100", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010100", 
            "name": "GM2 gangliosidosis, B, B1 variant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010100", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010100", 
            "name": "B variant GM2-gangliosidosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010100", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010100", 
            "name": "disease, Tay-Sachs"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010100", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010100", 
            "name": "Tay-Sachs disease, pseudo-Ab variant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010100", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010100", 
            "name": "TAY-Sachs disease; TSD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010100", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010100", 
            "name": "hexosaminidase a deficiency, adult type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010100", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010100", 
            "name": "sphingolipidosis, Tay-Sachs"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010100", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010100", 
            "name": "gangliosidosis GM2 , type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010100", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010100", 
            "name": "hexosaminidase alpha-subunit deficiency (variant B)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010100", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010100", 
            "name": "hexa deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:3320", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:3320", 
            "name": "GM2 gangliosidosis, type 1"
        }, 
        {
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            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:3320", 
            "name": "hexosaminidase A deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:3320", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:3320", 
            "name": "A GM2 gangliosidosis that is characterized the onset in infancy of developmental retardation, followed by paralysis, dementia and blindness, with death in the second or third year of life and has_material_basis_in homozygous or compound heterozygous mutation in the alpha subunit of the hexosaminidase A gene (HEXA) on chromosome 15q23."
        }, 
        {
            "url": "https://www.omim.org/entry/272800", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:272800", 
            "name": "GM2-gangliosidosis 1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:3320", 
        "description": "", 
        "resource": "Disease Ontology", 
        "id": "DOID:3320", 
        "name": "Tay-Sachs disease"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/272800", 
            "id": "272800", 
            "database": "MIM"
        }
    ]
}