{
    "disease_id": "DOID:0060979",
    "recommended_name": {
        "id": "DOID:0060979",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0060979",
        "name": "Fanconi anemia complementation group S",
        "description": "A Fanconi anemia characterized by developmental delay apparent from infancy, short stature, microcephaly, and coarse dysmorphic features that has_material_basis_in compound heterozygous or homozygous mutation in the BRCA1 gene on chromosome 17q21."
    },
    "synonyms": [
        {
            "id": "MONDO:0054748",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0054748",
            "name": "Fanconi anemia, complementation group S",
            "description": ""
        },
        {
            "id": "MONDO:0054748",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0054748",
            "name": "Fanconi anemia, complementation group S",
            "description": ""
        },
        {
            "id": "MONDO:0054748",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0054748",
            "name": "FANCS",
            "description": ""
        },
        {
            "id": "MONDO:0054748",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0054748",
            "name": "Fanconi anemia, complementation GROUP S",
            "description": ""
        },
        {
            "id": "MIM:617883",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/617883",
            "name": "Fanconi anemia, complementation group S",
            "description": "Fanconi anemia, complementation group S"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060979"
    ],
    "unlinked_id_list": []
}