{
    "disease_id": "DOID:0110961",
    "recommended_name": {
        "id": "DOID:0110961",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110961",
        "name": "atypical Gaucher's disease due to saposin c deficiency",
        "description": "A Gaucher's disease that has_material_basis_in compound heterozygous mutation in the PSAP gene on chromosome 10q22.1."
    },
    "synonyms": [
        {
            "id": "MONDO:0012517",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012517",
            "name": "Gaucher disease due to saposin C deficiency",
            "description": "Any Gaucher disease in which the cause of the disease is a mutation in the PSAP gene."
        },
        {
            "id": "MONDO:0012517",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012517",
            "name": "Gaucher disease caused by mutation in PSAP",
            "description": ""
        },
        {
            "id": "MONDO:0012517",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012517",
            "name": "PSAP Gaucher disease",
            "description": ""
        },
        {
            "id": "MONDO:0012517",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012517",
            "name": "atypical Gaucher disease due to saposin C deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0012517",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012517",
            "name": "atypical Gaucher's disease due to saposin c deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0012517",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012517",
            "name": "Gaucher disease, atypical",
            "description": ""
        },
        {
            "id": "MIM:610539",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/610539",
            "name": "Gaucher disease, atypical, due to saposin C deficiency",
            "description": "Gaucher disease, atypical, due to saposin C deficiency"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110961"
    ],
    "unlinked_id_list": []
}