{
    "disease_id": "DOID:0051009",
    "recommended_name": {
        "id": "DOID:0051009",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0051009",
        "name": "congenital nonspherocytic hemolytic anemia 10",
        "description": "A congenital nonspherocytic hemolytic anemia that has_material_basis_in homozygous or compound heterozygous mutation in the GSR gene on chromosome 8p21."
    },
    "synonyms": [
        {
            "id": "MONDO:0019531",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0019531",
            "name": "hemolytic anemia due to glutathione reductase deficiency",
            "description": "Haemolytic anemia due to glutathione reductase (GSR) deficiency is characterized by nearly complete absence of GSR activity in erythrocytes."
        },
        {
            "id": "MONDO:0019531",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0019531",
            "name": "hemolytic anemia due to glutathione reductase deficiency",
            "description": ""
        },
        {
            "id": "MIM:618660",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/618660",
            "name": "Anemia, congenital, non-spherocytic hemolytic, 10",
            "description": "Anemia, congenital, non-spherocytic hemolytic, 10"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0051009"
    ],
    "unlinked_id_list": []
}