{
  "id": 15517,
  "label": "platelet-type bleeding disorder 19",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0014518",
  "properties": {
    "xrefs": [
      "DOID:0111048",
      "GARD:0017738",
      "MEDGEN:863842",
      "OMIM:616176",
      "Orphanet:438207",
      "UMLS:C4015405"
    ],
    "synonyms": [
      "BDPLT19",
      "PRKACG isolated hereditary giant platelet disorder",
      "isolated hereditary giant platelet disorder caused by mutation in PRKACG",
      "severe autosomal recessive macrothrombocytopenia",
      "bleeding disorder, platelet-type, 19"
    ],
    "categories": [
      {
        "ref": "MONDO:0005570",
        "name": "hematologic disorder"
      }
    ],
    "definition": "Any isolated hereditary giant platelet disorder in which the cause of the disease is a mutation in the PRKACG gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 2702,
      "label": "inherited bleeding disorder, platelet-type",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4360,
        4362,
        5714
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:2218",
          "GARD:0022702",
          "MEDGEN:610",
          "OMIMPS:231200",
          "UMLS:C0005818"
        ],
        "synonyms": [
          "blood platelet disease",
          "platelet disorder",
          "bleeding disorder, platelet-type",
          "thrombocytopathy"
        ],
        "categories": [
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ]
      },
      "child_count": 84,
      "reference_id": "MONDO:0000009"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 2702,
      "label": "inherited bleeding disorder, platelet-type"
    }
  ]
}