{
    "disease_id": "DOID:0111905", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013791", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013791", 
            "name": "thrombophilia due to protein S deficiency, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013791", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013791", 
            "name": "THPH6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013791", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013791", 
            "name": "thrombophilia due to PROTEIN S deficiency, autosomal recessive; THPH6"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111905", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111905", 
            "name": "THPH6"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111905", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111905", 
            "name": "severe hereditary thrombophilia due to congenital protein S deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111905", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111905", 
            "name": "autosomal recessive thrombophilia due to congenital protein S deficiency"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111905", 
        "description": "A protein S deficiency characterized by thrombosis and secondary hemorrhage usually beginning in early infancy that has_material_basis_in homozygous or compound heterozygous mutation in PROS1 on chromosome 3q11.1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111905", 
        "name": "autosomal recessive thrombophilia due to protein S deficiency"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111905#disease-associations", 
            "id": "0111905", 
            "database": "Alliance of Genome Resources"
        }
    ]
}