{
  "id": 12343,
  "label": "amyotrophic lateral sclerosis type 4",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0011223",
  "properties": {
    "xrefs": [
      "DOID:0060196",
      "GARD:0010502",
      "MEDGEN:355983",
      "MESH:C566550",
      "OMIM:602433",
      "Orphanet:357043",
      "UMLS:C1865409"
    ],
    "synonyms": [
      "ALS 4",
      "ALS4",
      "SETX amyotrophic lateral sclerosis",
      "amyotrophic lateral sclerosis 4, juvenile",
      "amyotrophic lateral sclerosis caused by mutation in SETX",
      "dHMN with upper motor neuron signs",
      "distal hereditary motor neuropathy with upper motor neuron signs",
      "neuronopathy, distal hereditary motor, with pyramidal features"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Any amyotrophic lateral sclerosis in which the cause of the disease is a mutation in the SETX gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 6868,
      "label": "familial amyotrophic lateral sclerosis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6718,
        21302
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "EFO:0001356",
          "GARD:0024155",
          "MEDGEN:1642547",
          "OMIMPS:105400",
          "UMLS:C4551993"
        ],
        "synonyms": [
          "hereditary amyotrophic lateral sclerosis"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "An instance of amyotrophic lateral sclerosis that is caused by an inherited modification of the individual's genome."
      },
      "child_count": 60,
      "reference_id": "MONDO:0005144"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 6868,
      "label": "familial amyotrophic lateral sclerosis"
    }
  ]
}