{
    "disease_id": "DOID:0111051", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014386", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014386", 
            "name": "bleeding disorder, platelet-type, 18; BDPLT18"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014386", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014386", 
            "name": "bleeding disorder due to calcium- and DAG-regulated guanine exchange factor-1 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014386", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014386", 
            "name": "BDPLT18"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014386", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014386", 
            "name": "RASGRP2 inherited bleeding disorder, platelet-type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014386", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014386", 
            "name": "inherited bleeding disorder, platelet-type caused by mutation in RASGRP2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014386", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014386", 
            "name": "bleeding disorder due to CalDAG-GEFI deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014386", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014386", 
            "name": "bleeding disorder, platelet-type, 18"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111051", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111051", 
            "name": "BDPLT18"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111051", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111051", 
            "name": "bleeding disorder due to CalDAG-GEFI deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111051", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111051", 
            "name": "bleeding disorder due to calcium- and DAG-regulated guanine exchange factor-1 deficiency"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111051", 
        "description": "A blood platelet disease characterized by autosomal recessive inheritance of mucocutaneous bleeding, prolonged and severe epistaxis, hematomas and bleeding after tooth extraction that has_material_basis_in homozygous mutation in the RASGRP2 gene on chromosome 11q13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111051", 
        "name": "platelet-type bleeding disorder 18"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111051#disease-associations", 
            "id": "0111051", 
            "database": "Alliance of Genome Resources"
        }
    ]
}