{
  "id": 26357,
  "label": "fetomaternal alloimmune thrombocytopenia 2",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0980724",
  "properties": {
    "xrefs": [
      "OMIM:621266"
    ],
    "categories": [
      {
        "ref": "MONDO:0005570",
        "name": "hematologic disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 19243,
      "label": "fetal and neonatal alloimmune thrombocytopenia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4360,
        5714
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0002295",
          "MEDGEN:1720701",
          "NANDO:2200647",
          "NORD:91170",
          "OMIMPS:621264",
          "Orphanet:853",
          "SCTID:240305000",
          "UMLS:C3854603"
        ],
        "synonyms": [
          "NAIT"
        ],
        "categories": [
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "A rare hematological disease characterized by maternal alloimmunisation against fetal platelet antigens that are inherited from the father and different from those present in the mother, and usually presents as a severe isolated thrombocytopenia in otherwise healthy newborns."
      },
      "child_count": 6,
      "reference_id": "MONDO:0019415"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 19243,
      "label": "fetal and neonatal alloimmune thrombocytopenia"
    }
  ]
}