{
  "id": 10683,
  "label": "Immunoerythromyeloid hypoplasia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0009456",
  "properties": {
    "xrefs": [
      "GARD:0024672",
      "OMIM:242880"
    ],
    "synonyms": [
      "Immunoerythromyeloid hypoplasia"
    ],
    "categories": [
      {
        "ref": "MONDO:0005046",
        "name": "immune system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 11174,
      "label": "reticular dysgenesis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18070,
        22249
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060020",
          "GARD:0008625",
          "MEDGEN:124417",
          "MESH:C538361",
          "NANDO:1200322",
          "NANDO:2200695",
          "NCIT:C27070",
          "OMIM:267500",
          "Orphanet:33355",
          "SCTID:111584000",
          "UMLS:C0272167"
        ],
        "synonyms": [
          "AK2 deficiency",
          "De Vaal disease",
          "SCID with leukopenia",
          "congenital aleukocytosis",
          "generalised haematopoietic hypoplasia",
          "generalized hematopoietic hypoplasia",
          "reticular dysgenesis",
          "severe combined immunodeficiency with leukopenia",
          "DeVaal disease",
          "RD",
          "congenital Aleukia",
          "haematopoietic hypoplasia, generalised",
          "hematopoietic hypoplasia, generalized",
          "reticular Dysgenesia"
        ],
        "categories": [
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "Reticular dysgenesis is the most severe form of severe combined immunodeficiency (SCID) and is characterized by bilateral sensorineural deafness and a lack of innate and adaptive immune functions leading to fatal septicemia within days after birth if not treated."
      },
      "child_count": 2,
      "reference_id": "MONDO:0009973"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 11174,
      "label": "reticular dysgenesis"
    }
  ]
}