{
    "disease_id": "DOID:0111058",
    "recommended_name": {
        "id": "DOID:0111058",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111058",
        "name": "platelet-type bleeding disorder 12",
        "description": "A blood platelet disease characterized by autosomal dominant inheritance of mildly increased bleeding,  platelet aggregation defect, and impaired conversion of arachidonic acid to thromboxane A2 in platelets due to deficiency in PTGS1 activity."
    },
    "synonyms": [
        {
            "id": "DOID:0111058",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111058",
            "name": "platelet prostaglandin-endoperoxide synthase 1 deficiency",
            "description": ""
        },
        {
            "id": "DOID:0111058",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111058",
            "name": "BDPLT12",
            "description": ""
        },
        {
            "id": "DOID:0111058",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111058",
            "name": "PGHS1 deficiency",
            "description": ""
        },
        {
            "id": "DOID:0111058",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111058",
            "name": "platelet COX1 deficiency",
            "description": ""
        },
        {
            "id": "DOID:0111058",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111058",
            "name": "platelet cyclooxygenase 1 deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0011588",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011588",
            "name": "platelet-type bleeding disorder 12",
            "description": "An inherited blood coagulation disease characterized by autosomal dominant inheritance of mildly increased bleeding, platelet aggregation defect, and impaired conversion of arachidonic acid to thromboxane A2 in platelets due to deficiency in PTGS1 activity."
        },
        {
            "id": "MONDO:0011588",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011588",
            "name": "prostaglandin-endoperoxide synthase 1 deficiency, platelet",
            "description": ""
        },
        {
            "id": "MONDO:0011588",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011588",
            "name": "platelet prostaglandin-endoperoxide synthase 1 deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0011588",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011588",
            "name": "platelet cyclooxygenase 1 deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0011588",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011588",
            "name": "PGHS1 deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0011588",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011588",
            "name": "bleeding disorder, platelet-type, 12; BDPLT12",
            "description": ""
        },
        {
            "id": "MONDO:0011588",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011588",
            "name": "platelet COX1 deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0011588",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011588",
            "name": "bleeding disorder, platelet-type, 12",
            "description": ""
        },
        {
            "id": "MONDO:0011588",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011588",
            "name": "BDPLT12",
            "description": ""
        }
    ]
}