{
  "id": 10053,
  "label": "juvenile amyotrophic lateral sclerosis with dementia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0008781",
  "properties": {
    "xrefs": [
      "DOID:0110067",
      "GARD:0024639",
      "MEDGEN:395347",
      "MESH:C565956",
      "OMIM:205200",
      "UMLS:C1859806"
    ],
    "synonyms": [
      "ALS-dementia complex",
      "ALS-dementia Complex",
      "amyotrophic lateral sclerosis, juvenile, with dementia"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "A juvenile amyotrophic lateral sclerosis that is slowly progressive with concomitantly progressive dementia."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 17873,
      "label": "juvenile amyotrophic lateral sclerosis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6868
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0011901",
          "MEDGEN:923704",
          "Orphanet:300605",
          "SCTID:718555006",
          "UMLS:C3468114"
        ],
        "synonyms": [
          "JALS",
          "juvenile Charcot disease",
          "juvenile Lou Gehrig disease",
          "amyotrophic lateral sclerosis, juvenile"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Juvenile amyotrophic lateral sclerosis (JALS) is a very rare severe motor neuron disease characterized by progressive upper and lower motor neuron degeneration causing facial spasticity, dysarthria, and gait disorders with onset before 25 years of age."
      },
      "child_count": 4,
      "reference_id": "MONDO:0017593"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 17873,
      "label": "juvenile amyotrophic lateral sclerosis"
    }
  ]
}