{
    "disease_id": "DOID:0110958",
    "recommended_name": {
        "id": "DOID:0110958",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110958",
        "name": "Gaucher's disease type II",
        "description": "A Gaucher's disease characterized by rapid neurologic deterioration with cranial nerve and extrapyramidal tract involvement that has_material_basis_in homozygous or compound heterozygous mutation in the GBA1 gene on chromosome 1q22."
    },
    "synonyms": [
        {
            "id": "DOID:0110958",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110958",
            "name": "GD II",
            "description": ""
        },
        {
            "id": "DOID:0110958",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110958",
            "name": "Gaucher Disease, Acute Neuronopathic Type",
            "description": ""
        },
        {
            "id": "DOID:0110958",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110958",
            "name": "Infantile Cerebral Gaucher Disease",
            "description": ""
        },
        {
            "id": "DOID:0110958",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110958",
            "name": "GD2",
            "description": ""
        },
        {
            "id": "MONDO:0009266",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009266",
            "name": "Gaucher disease type II",
            "description": "Gaucher disease type 2 is the acute neurological form of Gaucher disease (GD). It is characterized by early-onset and severe neurological involvement of the brainstem, associated with an organomegaly and generally leading to death before the age of 2."
        },
        {
            "id": "MONDO:0009266",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009266",
            "name": "Gaucher disease type II",
            "description": ""
        },
        {
            "id": "MONDO:0009266",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009266",
            "name": "Gaucher disease, acute neuronopathic type",
            "description": ""
        },
        {
            "id": "MONDO:0009266",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009266",
            "name": "Gaucher's disease type II",
            "description": ""
        },
        {
            "id": "MONDO:0009266",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009266",
            "name": "acute neuronopathic Gaucher disease",
            "description": ""
        },
        {
            "id": "MONDO:0009266",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009266",
            "name": "infantile cerebral Gaucher disease",
            "description": ""
        },
        {
            "id": "MONDO:0009266",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009266",
            "name": "Gaucher disease, infantile cerebral",
            "description": ""
        },
        {
            "id": "MIM:230900",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/230900",
            "name": "Gaucher disease 2",
            "description": "Gaucher disease 2"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110958"
    ],
    "unlinked_id_list": []
}