{
    "disease_id": "DOID:0110957",
    "recommended_name": {
        "id": "DOID:0110957",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110957",
        "name": "Gaucher's disease type I",
        "description": "A Gaucher's disease characterized by absence of primary central nervous system involvement that has_material_basis_in a mutation of GBA on chromosome 1q22."
    },
    "synonyms": [
        {
            "id": "DOID:0110957",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110957",
            "name": "GD1",
            "description": ""
        },
        {
            "id": "DOID:0110957",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110957",
            "name": "Acid Beta-Glucosidase Deficiency",
            "description": ""
        },
        {
            "id": "DOID:0110957",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110957",
            "name": "GD I",
            "description": ""
        },
        {
            "id": "DOID:0110957",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110957",
            "name": "Gaucher Disease, Noncerebral Juvenile",
            "description": ""
        },
        {
            "id": "DOID:0110957",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110957",
            "name": "Gba Deficiency",
            "description": ""
        },
        {
            "id": "DOID:0110957",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110957",
            "name": "Glucocerebrosidase Deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009265",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009265",
            "name": "Gaucher disease type I",
            "description": "Gaucher disease type 1 is the chronic non-neurological form of Gaucher disease (GD; see this term) characterized by organomegaly, bone involvement and cytopenia."
        },
        {
            "id": "MONDO:0009265",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009265",
            "name": "Gaucher's disease type I",
            "description": ""
        },
        {
            "id": "MONDO:0009265",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009265",
            "name": "acid Beta-glucosidase deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009265",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009265",
            "name": "Gaucher disease type 1",
            "description": ""
        },
        {
            "id": "MONDO:0009265",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009265",
            "name": "Gaucher disease, type I",
            "description": ""
        },
        {
            "id": "MONDO:0009265",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009265",
            "name": "Gd 1",
            "description": ""
        },
        {
            "id": "MONDO:0009265",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009265",
            "name": "non-cerebral juvenile Gaucher disease",
            "description": ""
        },
        {
            "id": "MONDO:0009265",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009265",
            "name": "Gba deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009265",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009265",
            "name": "Gaucher disease, type 1",
            "description": ""
        },
        {
            "id": "MONDO:0009265",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009265",
            "name": "glucocerebrosidase deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009265",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009265",
            "name": "GD I",
            "description": ""
        },
        {
            "id": "MONDO:0009265",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009265",
            "name": "Gaucher disease, noncerebral juvenile",
            "description": ""
        },
        {
            "id": "MIM:230800",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/230800",
            "name": "Gaucher disease 1",
            "description": "Gaucher disease 1"
        }
    ]
}