{
    "disease_id": "DOID:0111401", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009134", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009134", 
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        }, 
        {
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            "description": "", 
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        }, 
        {
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        }, 
        {
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            "description": "", 
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        }, 
        {
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            "description": "", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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            "name": "SEC23B-CDG"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009134", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009134", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009134", 
            "name": "hempas anemia"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009134", 
            "name": "dyserythropoietic Anemia, hempas type"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009134", 
            "name": "anemia, congenital dyserythropoietic, type 2"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009134", 
            "name": "hereditary erythroblastic multinuclearity with Positive acidified-serum test"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009134", 
            "description": "", 
            "resource": "MONDO", 
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            "name": "CDA II"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111401", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111401", 
            "name": "CDA II"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111401", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111401", 
            "name": "CDA type 2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111401", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111401", 
            "name": "CDA type II"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111401", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111401", 
            "name": "CDAN2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111401", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111401", 
            "name": "Congenital dyserythropoietic anaemia type 2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111401", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111401", 
            "name": "Congenital dyserythropoietic anemia type 2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111401", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111401", 
            "name": "SEC23B-CDG"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111401", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111401", 
            "name": "congenital dyserythropoietic anaemia type II"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111401", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111401", 
            "name": "Hereditary erythroblastic multinuclearity with a positive acidified-serum test (hempas)"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111401", 
        "description": "A congenital dyserythropoietic anemia characterized by mild to severe anemia, bi- and multinucleated erythroblasts in bone marrow, jaundice and splenomegaly and may lead to liver iron overload and gallstones that has_material_basis_in homozygous or compound heterozygous mutation in SEC23B on chromosome 20p11.23.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111401", 
        "name": "congenital dyserythropoietic anemia type II"
    }, 
    "evidence": [
        {
            "url": "https://glycosmos.org/glycogenes/show?source=kegg&gene_id=10483", 
            "id": "10483", 
            "database": "GlyCosmos"
        }
    ]
}