{
  "id": 9276,
  "label": "jaw-winking syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007946",
  "properties": {
    "xrefs": [
      "DOID:560",
      "GARD:0006972",
      "ICD9:374.43",
      "ICD9:742.8",
      "MEDGEN:120582",
      "MESH:C535908",
      "MedDRA:10064583",
      "NORD:1401",
      "OMIM:154600",
      "Orphanet:91412",
      "SCTID:5127009",
      "UMLS:C0266521",
      "icd11.foundation:590216180"
    ],
    "synonyms": [
      "Marcus Gunn Phenomenon",
      "Marcus Gunn phenomenon",
      "Marcus Gunn syndrome",
      "Marcus-Gunn phenomenon",
      "Marcus-Gunn syndrome",
      "Maxillopalpebral synkinesis",
      "jaw-winking",
      "jaw-winking syndrome",
      "mandibulo-palpebral synkinesis-ptosis syndrome",
      "abnormal innervation syndrome of eyelid",
      "familial Marcus Gunn phenomenon (subtype)"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      },
      {
        "ref": "MONDO:0024458",
        "name": "disorder of visual system"
      }
    ],
    "definition": "Marcus-Gunn syndrome is characterized by ptosis associated with maxillopalpebral synkinesis."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 4370,
      "label": "syndromic disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29379
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:225",
          "MEDGEN:11688",
          "MESH:D013577",
          "NCIT:C28193",
          "OGMS:0000086",
          "UMLS:C0039082"
        ],
        "synonyms": [
          "cluster, symptom",
          "clusters, symptom",
          "symptom cluster",
          "symptom clusters",
          "syndrome",
          "syndrome associated with disease or disorder",
          "syndromes",
          "syndromic disease",
          "syndromic disease or disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "A group of signs, symptoms, and clinicopathological characteristics that may or may not have a genetic basis and collectively define an abnormal condition."
      },
      "child_count": 1182,
      "reference_id": "MONDO:0002254"
    },
    {
      "id": 5469,
      "label": "cranial nerve neuropathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6799
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:5656",
          "ICD9:352.9",
          "MEDGEN:1160",
          "MESH:D003389",
          "NCIT:C26733",
          "SCTID:73013002",
          "UMLS:C0010266"
        ],
        "synonyms": [
          "cranial nerve disease",
          "cranial nerve disorder",
          "cranial neuron projection bundle disease",
          "cranial neuron projection bundle disease or disorder",
          "cranial neuropathy",
          "disease of cranial neuron projection bundle",
          "disease or disorder of cranial neuron projection bundle",
          "disorder of cranial nerve",
          "disorder of cranial neuron projection bundle"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A neoplastic or non-neoplastic disorder that affects one of the cranial nerves."
      },
      "child_count": 17,
      "reference_id": "MONDO:0003569"
    },
    {
      "id": 21415,
      "label": "disorder of visual system",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29379
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "SCTID:128127008"
        ],
        "synonyms": [
          "disease of visual system",
          "disease or disorder of visual system",
          "disorder of visual system",
          "visual system disease",
          "visual system disease or disorder",
          "visual system disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "A disease that involves the visual system."
      },
      "child_count": 30,
      "reference_id": "MONDO:0024458"
    }
  ],
  "children": [
    {
      "id": 16066,
      "label": "Marin-Amat syndrome",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        9276
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019779",
          "MEDGEN:1842834",
          "Orphanet:101104",
          "UMLS:C5681802",
          "icd11.foundation:727922687"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0015101"
    },
    {
      "id": 19823,
      "label": "inverse Marcus-Gunn phenomenon",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        9276
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019608",
          "MEDGEN:1784220",
          "Orphanet:98951",
          "UMLS:C5548210",
          "icd11.foundation:348052110"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "Inverse Marcus-Gunn phenomenon is a rare congenital synkinesis where jaw opening by the pterygoid muscle (during eating or yawning) causes eyelid drooping from inhibition of the oculomotor nerve to the levator palpebrae superioris. Familial occurrence has been reported."
      },
      "child_count": 0,
      "reference_id": "MONDO:0020362"
    }
  ],
  "roots": [
    {
      "id": 4370,
      "label": "syndromic disease"
    },
    {
      "id": 5469,
      "label": "cranial nerve neuropathy"
    },
    {
      "id": 21415,
      "label": "disorder of visual system"
    }
  ]
}