{
  "id": 10908,
  "label": "myeloperoxidase deficiency",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0009694",
  "properties": {
    "xrefs": [
      "GARD:0003868",
      "ICD9:288.8",
      "MEDGEN:96015",
      "MESH:C562864",
      "NANDO:1200358",
      "NANDO:2200758",
      "OMIM:254600",
      "Orphanet:2587",
      "SCTID:234433009",
      "UMLS:C0398595",
      "icd11.foundation:1933575033"
    ],
    "synonyms": [
      "MPO deficiency",
      "myeloperoxidase deficiency",
      "MPOD"
    ],
    "categories": [
      {
        "ref": "MONDO:0005046",
        "name": "immune system disorder"
      },
      {
        "ref": "MONDO:0005570",
        "name": "hematologic disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 5714,
      "label": "hereditary disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29382
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:630",
          "EFO:0000508",
          "ICD9:799.89",
          "MEDGEN:5527",
          "MESH:D030342",
          "NCIT:C3101",
          "SCTID:32895009",
          "UMLS:C0019247"
        ],
        "synonyms": [
          "genetic condition",
          "genetic disease",
          "genetic disorder",
          "hereditary disease",
          "hereditary disease or disorder",
          "hereditary diseases",
          "inherited disease",
          "inherited genetic disease",
          "molecular disease",
          "Mendelian disease",
          "familial disorder",
          "inborn disorder"
        ],
        "definition": "A disease that is caused by genetic modifications where those modifications are inherited from a parent's genome."
      },
      "child_count": 1925,
      "reference_id": "MONDO:0003847"
    },
    {
      "id": 16630,
      "label": "functional neutrophil defect",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6569
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020321",
          "MEDGEN:1863601",
          "Orphanet:183681",
          "SCTID:105600002",
          "UMLS:C5924997",
          "icd11.foundation:808756909"
        ],
        "synonyms": [
          "neutrophil disease",
          "neutrophilopathy"
        ],
        "categories": [
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          },
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ]
      },
      "child_count": 5,
      "reference_id": "MONDO:0015978"
    },
    {
      "id": 21540,
      "label": "defective phagocytic cell engulfment",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        21541
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:585050",
          "SCTID:234585008",
          "UMLS:C0398742"
        ],
        "synonyms": [
          "defective phagocytic cell killing"
        ],
        "categories": [
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ]
      },
      "child_count": 5,
      "reference_id": "MONDO:0024626"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 5714,
      "label": "hereditary disease"
    },
    {
      "id": 16630,
      "label": "functional neutrophil defect"
    },
    {
      "id": 21540,
      "label": "defective phagocytic cell engulfment"
    }
  ]
}