{
    "disease_id": "DOID:0060065", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008785", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008785", 
            "name": "sideroblastic anemia 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008785", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008785", 
            "name": "pyridoxine refractory sideroblastic anemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008785", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008785", 
            "name": "anemia, sideroblastic, 2, pyridoxine-refractory; SIDBA2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008785", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008785", 
            "name": "anemia, sideroblastic, pyridoxine-refractory, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008785", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008785", 
            "name": "sideroblastic anemia pyridoxine-refractory autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008785", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008785", 
            "name": "anemia, sideroblastic, 2, pyridoxine-refractory"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008785", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008785", 
            "name": "SIDBA2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060065", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060065", 
            "name": "pyridoxine-refractory autosomal recessive sideroblastic anaemia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060065", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060065", 
            "name": "autosomal recessive pyridoxine-refractory sideroblastic anaemia 2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060065", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060065", 
            "name": "pyridoxine-refractory autosomal recessive sideroblastic anemia"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060065", 
        "description": "A sideroblastic anemia that is characterized by microcytic hypochromic anemia and iron overload, and has_material_basis_in autosomal recessive inheritance of mutation in the SLC25A38 gene.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060065", 
        "name": "autosomal recessive pyridoxine-refractory sideroblastic anemia 2"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060065#disease-associations", 
            "id": "0060065", 
            "database": "Alliance of Genome Resources"
        }
    ]
}