{
  "id": 15560,
  "label": "neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0014562",
  "properties": {
    "xrefs": [
      "DOID:0070244",
      "GARD:0017796",
      "MEDGEN:1799985",
      "OMIM:616276",
      "Orphanet:457185",
      "UMLS:C5568562"
    ],
    "synonyms": [
      "COQ4-related neonatal encephalomyopathy",
      "coenzyme Q10 deficiency, primary, type 7",
      "COQ10D7",
      "coenzyme Q10 deficiency, primary, 7",
      "primary coenzyme Q10 deficiency 7"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 18296,
      "label": "coenzyme Q10 deficiency",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16918,
        19748
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050730",
          "GARD:0010423",
          "MEDGEN:334528",
          "MESH:C564403",
          "NCIT:C142083",
          "OMIMPS:607426",
          "Orphanet:35656",
          "SCTID:724575009",
          "UMLS:C1843920",
          "icd11.foundation:1251664337"
        ],
        "synonyms": [
          "CoQ10 deficiency",
          "coenzyme Q10 deficiency disease",
          "coenzyme Q10 deficiency, primary",
          "CoQ10 deficiency, primary"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A genetically heterogeneous condition, typically inherited in an autosomal recessive fashion, characterized by coenzyme Q10 deficiency."
      },
      "child_count": 20,
      "reference_id": "MONDO:0018151"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 18296,
      "label": "coenzyme Q10 deficiency"
    }
  ]
}