{
  "id": 24059,
  "label": "Glanzmann thrombasthenia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0100326",
  "properties": {
    "xrefs": [
      "GARD:0002478",
      "MEDGEN:52736",
      "NORD:1186",
      "OMIMPS:273800",
      "Orphanet:849",
      "UMLS:C0040015",
      "icd11.foundation:1927726560"
    ],
    "synonyms": [
      "Glanzmann thrombasthenia"
    ],
    "categories": [
      {
        "ref": "MONDO:0005570",
        "name": "hematologic disorder"
      }
    ]
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "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"
    },
    {
      "id": 20411,
      "label": "inherited blood coagulation disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3738,
        5714
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:2214",
          "GARD:0020319",
          "MEDGEN:163105",
          "MESH:D025861",
          "Orphanet:183654",
          "UMLS:C0852077"
        ],
        "synonyms": [
          "coagulation disorder, hereditary",
          "coagulation disorder, inherited",
          "coagulation disorders, hereditary",
          "coagulation disorders, inherited",
          "hereditary blood coagulation disease",
          "hereditary blood coagulation disorders",
          "hereditary coagulation disorder",
          "hereditary coagulation disorders",
          "inherited blood coagulation disorders",
          "inherited coagulation disorder",
          "inherited coagulation disorders",
          "rare genetic coagulation disorder",
          "inherited blood coagulation disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "Hemorrhagic and thrombotic disorders that occur as a consequence of inherited abnormalities in blood coagulation."
      },
      "child_count": 78,
      "reference_id": "MONDO:0021181"
    }
  ],
  "children": [
    {
      "id": 22193,
      "label": "Glanzmann thrombasthenia 2",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        24059
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0016439",
          "MEDGEN:1782592",
          "OMIM:619267",
          "UMLS:C5543273"
        ],
        "synonyms": [
          "GT2",
          "Glanzmann thrombasthenia 2",
          "bleeding disorder, platelet-type, 23"
        ],
        "categories": [
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0031009"
    },
    {
      "id": 22236,
      "label": "Glanzmann thrombasthenia 1",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        24059
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:2219",
          "GARD:0015240",
          "MESH:D013915",
          "NCIT:C61249",
          "OMIM:273800",
          "SCTID:32942005"
        ],
        "synonyms": [
          "Glanzmann thrombasthenia",
          "Glanzmann's thrombasthenia",
          "BDPLT2",
          "Glanzmann thrombasthenia 1",
          "platelet glycoprotein IIb-IIIa deficiency",
          "thrombasthenia",
          "thrombasthenia of Glanzmann and Naegeli",
          "Diacyclothrombopathia 2B 3A",
          "GP IIb-IIIa Complex, deficiency of",
          "GT",
          "Glanzmann thrombasthenia type A",
          "Platelet fibrinogen receptor, deficiency of",
          "Platelet glycoprotein 2B 3A deficiency",
          "Platelet glycoprotein IIb-IIIa deficiency",
          "bleeding disorder, Platelet-type, 2",
          "deficiency of GP 2B 3A complex",
          "glycoprotein Complex IIb-IIIa, deficiency of"
        ],
        "categories": [
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "A bleeding syndrome characterized by spontaneous mucocutaneous bleeding and an exaggerated response to trauma due to a constitutional thrombocytopenia"
      },
      "child_count": 0,
      "reference_id": "MONDO:0031332"
    }
  ],
  "roots": [
    {
      "id": 2702,
      "label": "inherited bleeding disorder, platelet-type"
    },
    {
      "id": 20411,
      "label": "inherited blood coagulation disorder"
    }
  ]
}