{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014285", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014285", 
            "name": "congenital dyserythropoietic anemia type type 1B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014285", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014285", 
            "name": "anemia, congenital dyserythropoietic, type IB"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014285", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014285", 
            "name": "CDA, type IB"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014285", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014285", 
            "name": "CDAN1B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014285", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014285", 
            "name": "anemia, congenital dyserythropoietic, type IB; CDAN1B"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111397", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111397", 
            "name": "CDA, type Ib"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111397", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111397", 
            "name": "CDAN1B"
        }, 
        {
            "url": "https://www.omim.org/entry/615631", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:615631", 
            "name": "Anemia, congenital dyserythropoietic, 1B"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111397", 
        "description": "A congenital dyserythropoietic anemia type I that has_material_basis_in homozygous or compound heterozygous mutation in C15orf41 on chromosome 15q14.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111397", 
        "name": "congenital dyserythropoietic anemia type Ib"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/615631", 
            "id": "615631", 
            "database": "MIM"
        }
    ]
}