{
    "disease_id": "DOID:0051002",
    "recommended_name": {
        "id": "DOID:0051002",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0051002",
        "name": "congenital dyserythropoietic anemia type IVb",
        "description": "A congenital dyserythropoietic anemia characterized by neonatal jaundice, hyperbilirubinemia, and severe congenital hemolytic anemia requiring transfusionn and that has_material_basis_in homozygous or compound heterozygous mutation in the KLF1 gene on chromosome 19p13.13."
    },
    "synonyms": [
        {
            "id": "MONDO:0975829",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0975829",
            "name": "anemia, congenital dyserythropoietic, type IVb",
            "description": ""
        },
        {
            "id": "MIM:620969",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/620969",
            "name": "Anemia, congenital dyserythropoietic, 4B",
            "description": "Anemia, congenital dyserythropoietic, 4B"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0051002"
    ],
    "unlinked_id_list": []
}