{
  "id": 9397,
  "label": "amyotrophic neuralgia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0008076",
  "properties": {
    "xrefs": [
      "DOID:10383",
      "GARD:0003955",
      "ICD9:353.5",
      "MEDGEN:320318",
      "OMIM:162100",
      "SCTID:26609002",
      "UMLS:C1834304"
    ],
    "synonyms": [
      "amyotrophy, hereditary neuralgic",
      "amyotrophy, hereditary neuralgic, with predilection for brachial plexus",
      "brachial plexus neuropathy, hereditary",
      "hereditary brachial plexus neuropathy",
      "hereditary neuralgic amyotrophy",
      "neuritis with brachial predilection",
      "HNA",
      "neuralgic amyotrophy"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "An autosomal dominant form of recurrent focal neuropathy characterized clinically by acute, recurrent episodes of brachial plexus neuropathy with muscle weakness and atrophy preceded by severe pain in the affected arm."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 8150,
      "label": "brachial plexus neuropathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        21410
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:3690",
          "EFO:1000844",
          "GARD:0024459",
          "ICD9:353.0",
          "MEDGEN:148580",
          "MESH:D020516",
          "NCIT:C27194",
          "SCTID:3548001",
          "UMLS:C0700251"
        ],
        "synonyms": [
          "brachial nerve plexus peripheral neuropathy",
          "brachial plexopathy",
          "peripheral neuropathy of brachial nerve plexus"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A brachial plexus disorder characterized by regional paresthesia, pain and muscle weakness, and limited movement in the arm or hand."
      },
      "child_count": 7,
      "reference_id": "MONDO:0006683"
    },
    {
      "id": 19748,
      "label": "hereditary peripheral neuropathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6950,
        24271
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0010711",
          "MEDGEN:1825937",
          "Orphanet:98497",
          "UMLS:C5681733"
        ],
        "synonyms": [
          "genetic peripheral neuropathy"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "An instance of peripheral neuropathy that is caused by an inherited genomic modification in an individual."
      },
      "child_count": 130,
      "reference_id": "MONDO:0020127"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 8150,
      "label": "brachial plexus neuropathy"
    },
    {
      "id": 19748,
      "label": "hereditary peripheral neuropathy"
    }
  ]
}