{
    "disease_id": "DOID:12259", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010604", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010604", 
            "name": "congenital factor IX deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010604", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010604", 
            "name": "factor 9 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010604", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010604", 
            "name": "congenital factor IX disorder"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010604", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010604", 
            "name": "hereditary Factor IX deficiency disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010604", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010604", 
            "name": "hemophilia B(M)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010604", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010604", 
            "name": "HEMB"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010604", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010604", 
            "name": "plasma thromboplastin component deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010604", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010604", 
            "name": "deficiency, functional factor IX"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010604", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010604", 
            "name": "hemophilia type B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010604", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010604", 
            "name": "hemophilia B; HEMB"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010604", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010604", 
            "name": "hem B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010604", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010604", 
            "name": "hemophilia B Leyden"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010604", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010604", 
            "name": "factor IX deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010604", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010604", 
            "name": "F9 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010604", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010604", 
            "name": "hereditary Factor IX deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010604", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010604", 
            "name": "Christmas disease"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:12259", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:12259", 
            "name": "Congenital factor IX deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:12259", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:12259", 
            "name": "Congenital factor IX disorder"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:12259", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:12259", 
            "name": "deficiency, functional factor IX"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:12259", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:12259", 
            "name": "factor IX deficiency"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:12259", 
        "description": "A blood coagulation disease that has_material_basis_in Factor IX deficiency, which makes coagulation much more prolonged. The disease is inherited as an X-linked recessive trait.", 
        "resource": "Disease Ontology", 
        "id": "DOID:12259", 
        "name": "hemophilia B"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/12259#disease-associations", 
            "id": "12259", 
            "database": "Alliance of Genome Resources"
        }
    ]
}