{
  "id": 25056,
  "label": "TUBB4A-related neurologic disorder",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0800470",
  "properties": {
    "xrefs": [
      "GARD:0026570"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Any neurologic condition in which the cause of the disease is a mutation in the TUBB4A gene."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 1,
  "parents": [
    {
      "id": 21292,
      "label": "inherited neurodegenerative disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7208,
        24270
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020280",
          "MEDGEN:1825988",
          "MESH:D020271",
          "NCIT:C97073",
          "Orphanet:183500",
          "UMLS:C5680568"
        ],
        "synonyms": [
          "genetic neurodegenerative disease",
          "hereditary neurodegenerative disease",
          "hereditary neurodegenerative disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "An inherited disorder characterized by progressive degeneration and atrophy of the nervous system."
      },
      "child_count": 164,
      "reference_id": "MONDO:0024237"
    }
  ],
  "children": [
    {
      "id": 13945,
      "label": "hypomyelinating leukodystrophy 6",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        18952,
        25056
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060798",
          "GARD:0010917",
          "MEDGEN:436642",
          "MESH:C567314",
          "NANDO:1200578",
          "NANDO:2201290",
          "OMIM:612438",
          "Orphanet:139441",
          "UMLS:C2676244"
        ],
        "synonyms": [
          "H-ABC",
          "HABC",
          "HLD6",
          "hypomyelinating leukodystrophy type 6",
          "hypomyelination with atrophy of basal ganglia and cerebellum",
          "leukodystrophy, hypomyelinating, type 6",
          "leukodystrophy, hypomyelinating, 6",
          "leukodystrophy, hypomyelinating, with atrophy of the basal ganglia and cerebellum"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A leukodystrophy characterized by slowly progressive spasticity, extrapyramidal movement disorders (dystonia, choreoathetosis and rigidity), cerebellar ataxia, moderate to severe cognitive deficit, and anarthria/dysarthria."
      },
      "child_count": 0,
      "reference_id": "MONDO:0012905"
    }
  ],
  "roots": [
    {
      "id": 21292,
      "label": "inherited neurodegenerative disorder"
    }
  ]
}