{
    "disease_id": "DOID:0080343", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014804", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014804", 
            "name": "sideroblastic anemia 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014804", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014804", 
            "name": "GLRX5-related sideroblastic anemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014804", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014804", 
            "name": "anemia, sideroblastic, 3, pyridoxine-refractory; SIDBA3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014804", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014804", 
            "name": "adult-onset autosomal recessive sideroblastic anemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014804", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014804", 
            "name": "anemia, sideroblastic, 3, pyridoxine-refractory"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014804", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014804", 
            "name": "SIDBA3"
        }, 
        {
            "url": "https://www.omim.org/entry/616860", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:616860", 
            "name": "Anemia, sideroblastic, 3, pyridoxine-refractory"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080343", 
        "description": "A sideroblastic anemia that is characterized by homozygous or compound heterozygous mutation in the GLRX5 gene on chromosome 14q32.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080343", 
        "name": "autosomal recessive pyridoxine-refractory sideroblastic anemia 3"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/616860", 
            "id": "616860", 
            "database": "MIM"
        }
    ]
}