{
    "disease_id": "DOID:0111901", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012876", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012876", 
            "name": "heparin cofactor 2 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012876", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012876", 
            "name": "Hcf2 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012876", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012876", 
            "name": "thrombophilia due to heparin cofactor 2 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012876", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012876", 
            "name": "Hcf 2 deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111901", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111901", 
            "name": "THPH10"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111901", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111901", 
            "name": "HCF 2 deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111901", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111901", 
            "name": "HCF II deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111901", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111901", 
            "name": "thrombophilia due to heparin cofactor II deficiency"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111901", 
        "description": "A thrombophilia characterized by increased risk of thromboembolism that has_material_basis_in heterozygous mutation in HCF2 on chromosome 22q11.21.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111901", 
        "name": "heparin cofactor II deficiency"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111901#disease-associations", 
            "id": "0111901", 
            "database": "Alliance of Genome Resources"
        }
    ]
}