{
    "disease_id": "DOID:0111895", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007110", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007110", 
            "name": "DBA1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007110", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007110", 
            "name": "Blackfan-Diamond syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007110", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007110", 
            "name": "Diamond-Blackfan anemia 1; DBA1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007110", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007110", 
            "name": "aregenerative Anemia, chronic congenital"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007110", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007110", 
            "name": "Diamond-Blackfan Anemia type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007110", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007110", 
            "name": "Red cell aplasia, Pure, hereditary"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007110", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007110", 
            "name": "Aase syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007110", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007110", 
            "name": "anemia, congenital hypoplastic, of Blackfan and Diamond"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007110", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007110", 
            "name": "RPS19 Diamond-Blackfan anemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007110", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007110", 
            "name": "erythrogenesis imperfecta"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007110", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007110", 
            "name": "anemia, congenital erythroid hypoplastic"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007110", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007110", 
            "name": "DBA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007110", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007110", 
            "name": "Aase-Smith syndrome 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007110", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007110", 
            "name": "Diamond-Blackfan anemia caused by mutation in RPS19"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111895", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111895", 
            "name": "DBA1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111895", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111895", 
            "name": "RPS19-related Diamond-Blackfan anemia"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111895", 
        "description": "A Diamond-Blackfan anemia that has_material_basis_in heterozygous mutation in RPS19 on chromosome 19q13.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111895", 
        "name": "Diamond-Blackfan anemia 1"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/105650", 
            "id": "105650", 
            "database": "MIM"
        }
    ]
}