{
  "id": 8308,
  "label": "neonatal myasthenia gravis",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0006866",
  "properties": {
    "xrefs": [
      "DOID:14043",
      "GARD:0024493",
      "ICD9:775.2",
      "MEDGEN:102360",
      "MESH:D020941",
      "MedDRA:10028963",
      "SCTID:82178003",
      "UMLS:C0158982",
      "icd11.foundation:1274860004"
    ],
    "synonyms": [
      "neonatal myasthenia gravis"
    ],
    "categories": [
      {
        "ref": "MONDO:0005046",
        "name": "immune system disorder"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "A disorder of neuromuscular transmission that occurs in a minority of newborns born to women with myasthenia gravis. Clinical features are usually present at birth or develop in the first 3 days of life and consist of hypotonia and impaired respiratory, suck, and swallowing abilities. This condition is associated with the passive transfer of acetylcholine receptor antibodies through the placenta. In the majority of infants the myasthenic weakness resolves (i.e., transient neonatal myasthenia gravis) although this disorder may rarely continue beyond the neonatal period (i.e., persistent neonatal myasthenia gravis). (From Menkes, Textbook of Child Neurology, 5th ed, p823; Neurology 1997 Jan;48(1):50-4)"
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 10902,
      "label": "myasthenia gravis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3006
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:437",
          "EFO:0004991",
          "GARD:0007122",
          "ICD10CM:G70.0",
          "ICD9:358.0",
          "ICD9:358.00",
          "MEDGEN:7764",
          "MESH:D009157",
          "MedDRA:10028417",
          "NANDO:1200020",
          "NANDO:2100252",
          "NANDO:2200906",
          "NCIT:C60989",
          "NORD:1478",
          "OMIM:254200",
          "Orphanet:589",
          "SCTID:91637004",
          "UMLS:C0026896",
          "icd11.foundation:1270100227"
        ],
        "synonyms": [
          "acquired myasthenia",
          "autoimmune myasthenia gravis",
          "myasthenia gravis",
          "MG"
        ],
        "categories": [
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Myasthenia gravis (MG) is a rare, clinically heterogeneous, autoimmune disorder of the neuromuscular junction characterized by fatigable weakness of voluntary muscles."
      },
      "child_count": 6,
      "reference_id": "MONDO:0009688"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 10902,
      "label": "myasthenia gravis"
    }
  ]
}