{
    "disease_id": "DOID:0080502",
    "recommended_name": {
        "id": "DOID:0080502",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0080502",
        "name": "GM1 gangliosidosis type 1",
        "description": "A GM1 gangliosidosis that is characterized by rapid psychomotor deterioration beginning within 6 months of birth, generalized central nervous system involvement, hepatosplenomegaly, facial dysmorphism, macular cherry-red spots, skeletal dysplasia, and early death."
    },
    "synonyms": [
        {
            "id": "MONDO:0009260",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009260",
            "name": "GM1 gangliosidosis type 1",
            "description": "GM1 gangliosidosis type 1 is the severe infantile form of GM1 gangliosidosis with variable neurological and systemic manifestations."
        },
        {
            "id": "MONDO:0009260",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009260",
            "name": "Norman-Landing disease",
            "description": ""
        },
        {
            "id": "MONDO:0009260",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009260",
            "name": "infantile GM1 gangliosidosis",
            "description": ""
        },
        {
            "id": "MONDO:0009260",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009260",
            "name": "Beta galactosidase deficiency type 1",
            "description": ""
        },
        {
            "id": "MONDO:0009260",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009260",
            "name": "GLB deficiency type 1",
            "description": ""
        },
        {
            "id": "MONDO:0009260",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009260",
            "name": "gangliosidosis generalised GM1 infantile form",
            "description": ""
        },
        {
            "id": "MONDO:0009260",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009260",
            "name": "gangliosidosis generalised GM1 type 1",
            "description": ""
        },
        {
            "id": "MONDO:0009260",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009260",
            "name": "gangliosidosis generalized GM1 infantile form",
            "description": ""
        },
        {
            "id": "MONDO:0009260",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009260",
            "name": "gangliosidosis generalized GM1 type 1",
            "description": ""
        },
        {
            "id": "MONDO:0009260",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009260",
            "name": "gangliosidosis, generalised GM1, infantile form",
            "description": ""
        },
        {
            "id": "MONDO:0009260",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009260",
            "name": "gangliosidosis, generalised GM1, type 1",
            "description": ""
        },
        {
            "id": "MONDO:0009260",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009260",
            "name": "gangliosidosis, generalised GM1, type I, with Cardiac involvement",
            "description": ""
        },
        {
            "id": "MIM:230500",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/230500",
            "name": "GM1-gangliosidosis 1",
            "description": "GM1-gangliosidosis 1"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0080502"
    ],
    "unlinked_id_list": []
}