{
  "id": 24273,
  "label": "SERAC1-related neurological disorder",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0100548",
  "properties": {
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Any neurological disorder in which the cause of the disease is a mutation in the SERAC1 gene."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 1,
  "parents": [
    {
      "id": 24270,
      "label": "hereditary neurological disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        6799
      ],
      "type_id": 0,
      "properties": {
        "synonyms": [
          "neurogenetic disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A heterogeneous group of genetic conditions with Mendelian (autosomal dominant, recessive, or X-linked) or chromosomal etiology characterized by abnormalities in the brain, spinal cord, nerves, or muscles."
      },
      "child_count": 528,
      "reference_id": "MONDO:0100545"
    }
  ],
  "children": [
    {
      "id": 14887,
      "label": "3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        5908,
        17675,
        18270,
        24273
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110001",
          "GARD:0012963",
          "MEDGEN:873604",
          "OMIM:614739",
          "Orphanet:352328",
          "SCTID:711409002",
          "UMLS:C4040739"
        ],
        "synonyms": [
          "3-methylglutaconic aciduria caused by mutation in SERAC1",
          "3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome",
          "3-methylglutaconic aciduria with deafness-encephalopathy-Leigh-like syndrome",
          "MEGDEL",
          "MEGDEL syndrome",
          "MGCA6",
          "SERAC1 3-methylglutaconic aciduria",
          "3-MGCA type IV (formerly)",
          "3-MGCA-4 (formerly)",
          "3-Methylglutaconic aciduria with dystonia-deafness, hepatopathy, encephalopathy, and Leigh-like syndrome",
          "3-Methylglutaconic aciduria, type 6",
          "3-methylglutaconic aciduria type VI",
          "SERAC1 defect"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any 3-methylglutaconic aciduria in which the cause of the disease is a mutation in the SERAC1 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0013875"
    }
  ],
  "roots": [
    {
      "id": 24270,
      "label": "hereditary neurological disease"
    }
  ]
}