{
    "disease_id": "DOID:0080501",
    "recommended_name": {
        "id": "DOID:0080501",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0080501",
        "name": "GM1 gangliosidosis type 2",
        "description": "A GM1 gangliosidosis that is characterized by slowly progressive generalized neurodegeneration and mild skeletal changes, with onset between 7 months and 3 years of age."
    },
    "synonyms": [
        {
            "id": "DOID:0080501",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0080501",
            "name": "juvenile GM1 gangliosidosis",
            "description": ""
        },
        {
            "id": "MONDO:0009261",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009261",
            "name": "GM1 gangliosidosis type 2",
            "description": "GM1 gangliosidosis type 2 is a clinically variable, infancy or childhood-onset form of GM1 gangliosidosis characterized by normal early development and psychomotor regression between seven months and three years of age."
        },
        {
            "id": "MONDO:0009261",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009261",
            "name": "juvenile GM1 gangliosidosis",
            "description": ""
        },
        {
            "id": "MONDO:0009261",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009261",
            "name": "late-infantile GM1 gangliosidosis",
            "description": ""
        },
        {
            "id": "MONDO:0009261",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009261",
            "name": "gangliosidosis generalised GM1 juvenile type",
            "description": ""
        },
        {
            "id": "MONDO:0009261",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009261",
            "name": "gangliosidosis generalised GM1 type 2",
            "description": ""
        },
        {
            "id": "MONDO:0009261",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009261",
            "name": "gangliosidosis generalized GM1 juvenile type",
            "description": ""
        },
        {
            "id": "MONDO:0009261",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009261",
            "name": "gangliosidosis generalized GM1 type 2",
            "description": ""
        },
        {
            "id": "MONDO:0009261",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009261",
            "name": "gangliosidosis, generalised GM1, juvenile type",
            "description": ""
        },
        {
            "id": "MONDO:0009261",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009261",
            "name": "gangliosidosis, generalised GM1, late-infantile type",
            "description": ""
        },
        {
            "id": "MONDO:0009261",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009261",
            "name": "gangliosidosis, generalised GM1, type 2",
            "description": ""
        },
        {
            "id": "MIM:230600",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/230600",
            "name": "GM1-gangliosidosis 2",
            "description": "GM1-gangliosidosis 2"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0080501"
    ],
    "unlinked_id_list": []
}