{
    "disease_id": "DOID:0090016", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007925", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007925", 
            "name": "5Q minus syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007925", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007925", 
            "name": "myelodysplastic syndrome with 5q deletion"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007925", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007925", 
            "name": "5q deletion syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007925", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007925", 
            "name": "macrocytic Anemia, refractory, due to 5Q deletion"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007925", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007925", 
            "name": "MAR"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007925", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007925", 
            "name": "5q- syndrome, refractory macrocytic anemia due to 5q deletion"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007925", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007925", 
            "name": "5q- syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007925", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007925", 
            "name": "megakaryocytes, unilobular nucleated"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007925", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007925", 
            "name": "refractory macrocytic anemia due to 5q deletion"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007925", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007925", 
            "name": "5q syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007925", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007925", 
            "name": "myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007925", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007925", 
            "name": "myelodysplastic syndrome associated with isolated del (5q) chromosome Abnormality"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007925", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007925", 
            "name": "myelodysplastic syndrome with isolated del(5q)"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090016", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090016", 
            "name": "myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090016", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090016", 
            "name": "5q- syndrome, refractory macrocytic anemia due to 5q deletion"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0090016", 
        "description": "A chromosomal deletion syndrome characterized by severe macrocytic anemia erythroid hypoplasia in the bone marrow, hypolobated micromegakaryocytes and that has_material_basis_in somatic deletion of 1 allele of the RPS14, MIR145, MIR146A and/or DDX41 genes on chromosome 5q.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0090016", 
        "name": "chromosome 5q deletion syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0090016#disease-associations", 
            "id": "0090016", 
            "database": "Alliance of Genome Resources"
        }
    ]
}