{
  "id": 24814,
  "label": "immunodeficiency 105",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0800104",
  "properties": {
    "xrefs": [
      "DOID:0061074",
      "GARD:0026436",
      "MEDGEN:1809425",
      "OMIM:619924",
      "UMLS:C5677005"
    ],
    "synonyms": [
      "IMD105",
      "SCID, autosomal recessive, T cell-negative, B cell-positive, NK cell-positive",
      "severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, NK cell-positive"
    ],
    "categories": [
      {
        "ref": "MONDO:0005046",
        "name": "immune system disorder"
      }
    ],
    "definition": "Any immunodeficiency disease which the cause of the disease is a mutation in the PTPRC gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 22249,
      "label": "familial severe combined immunodeficiency",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16628
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0027938",
          "OMIMPS:601457"
        ],
        "categories": [
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ]
      },
      "child_count": 14,
      "reference_id": "MONDO:0031520"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 22249,
      "label": "familial severe combined immunodeficiency"
    }
  ]
}