{
    "disease_id": "DOID:0051004",
    "recommended_name": {
        "id": "DOID:0051004",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0051004",
        "name": "congenital nonspherocytic hemolytic anemia 3",
        "description": "A congenital nonspherocytic hemolytic anemia that has_material_basis_in homozygous or compound heterozygous mutation in the AK1 gene on chromosome 9q34."
    },
    "synonyms": [
        {
            "id": "MONDO:0012967",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012967",
            "name": "hemolytic anemia due to adenylate kinase deficiency",
            "description": "Hemolytic anemia due to adenylate kinase deficiency is a rare hemolytic anemia due to an erythrocyte nucleotide metabolism disorder characterized by moderate to severe chronic nonspherocytic hemolytic anemia that may require regular blood transfusions and/or splenectomy and may be associated with psychomotor impairment."
        },
        {
            "id": "MONDO:0012967",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012967",
            "name": "adenylate kinase deficiency, hemolytic anaemia due to",
            "description": ""
        },
        {
            "id": "MONDO:0012967",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012967",
            "name": "adenylate kinase deficiency, hemolytic anemia due to",
            "description": ""
        },
        {
            "id": "MIM:612631",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/612631",
            "name": "Anemia, congenital, non-spherocytic hemolytic, 3",
            "description": "Anemia, congenital, non-spherocytic hemolytic, 3"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0051004"
    ],
    "unlinked_id_list": []
}