{
  "id": 9300,
  "label": "Meniere disease",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007972",
  "properties": {
    "xrefs": [
      "DOID:9849",
      "EFO:0006862",
      "ICD9:386.0",
      "ICD9:386.00",
      "MEDGEN:7530",
      "MESH:D008575",
      "NCIT:C185243",
      "OMIM:156000",
      "Orphanet:45360",
      "SCTID:13445001",
      "UMLS:C0025281",
      "icd11.foundation:683932278"
    ],
    "synonyms": [
      "Meniere disease",
      "Meniere's disease"
    ],
    "categories": [
      {
        "ref": "MONDO:0002409",
        "name": "auditory system disorder"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      },
      {
        "ref": "MONDO:0024623",
        "name": "otorhinolaryngologic disease"
      }
    ],
    "definition": "A disease of the inner ear (labyrinth) that is characterized by fluctuating sensorineural hearing loss; tinnitus; episodic vertigo; and aural fullness. It is the most common form of endolymphatic hydrops."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 3,
  "parents": [
    {
      "id": 8201,
      "label": "endolymphatic hydrops",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6654
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:9848",
          "EFO:1000918",
          "ICD9:386.8",
          "MEDGEN:60183",
          "MESH:D018159",
          "MedDRA:10049934",
          "SCTID:27621000119100",
          "UMLS:C0206586"
        ],
        "categories": [
          {
            "ref": "MONDO:0002409",
            "name": "auditory system disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0024623",
            "name": "otorhinolaryngologic disease"
          }
        ],
        "definition": "An accumulation of endolymph in the inner ear (labyrinth) leading to buildup of pressure and distortion of intralabyrinthine structures, such as cochlea and semicircular canals. It is characterized by sensorineural hearing loss; tinnitus; and sometimes vertigo."
      },
      "child_count": 1,
      "reference_id": "MONDO:0006744"
    },
    {
      "id": 18718,
      "label": "hereditary otorhinolaryngologic disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        21538
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0021935",
          "MEDGEN:1842579",
          "Orphanet:466084",
          "UMLS:C5681130"
        ],
        "synonyms": [
          "genetic otorhinolaryngologic disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0024623",
            "name": "otorhinolaryngologic disease"
          }
        ],
        "definition": "An instance of otorhinolaryngologic disease that is caused by a modification of the individual's genome."
      },
      "child_count": 42,
      "reference_id": "MONDO:0018751"
    },
    {
      "id": 22991,
      "label": "inherited auditory system disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4499,
        5714
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:707712",
          "SCTID:362991006",
          "UMLS:C1285174"
        ],
        "synonyms": [
          "auditory system hereditary disorder",
          "hereditary auditory system disease",
          "inherited auditory system disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0002409",
            "name": "auditory system disorder"
          }
        ],
        "definition": "An instance of auditory system disease that is caused by an inherited modification of the individual's genome."
      },
      "child_count": 24,
      "reference_id": "MONDO:0037940"
    },
    {
      "id": 24271,
      "label": "hereditary neuromuscular disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18957,
        24270
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0026275"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A heterogeneous group of genetic conditions with Mendelian (autosomal dominant, recessive, or X-linked) or chromosomal etiology that is characterized by progressive muscle degeneration and weakness."
      },
      "child_count": 44,
      "reference_id": "MONDO:0100546"
    }
  ],
  "children": [
    {
      "id": 3914,
      "label": "active cochleovestibular Meniere disease",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        9300
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:13490",
          "ICD9:386.01",
          "MEDGEN:509989",
          "SCTID:194348002",
          "UMLS:C0155496"
        ],
        "synonyms": [
          "active Meniere's disease, cochleovestibular",
          "active cochleovestibular Meniere's disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0002409",
            "name": "auditory system disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0024623",
            "name": "otorhinolaryngologic disease"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0001727"
    },
    {
      "id": 3915,
      "label": "active vestibular Meniere disease",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        9300
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:13491",
          "ICD9:386.03",
          "MEDGEN:509991",
          "SCTID:194350005",
          "UMLS:C0155498"
        ],
        "synonyms": [
          "active Meniere's disease, vestibular",
          "active vestibular Meniere's disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0002409",
            "name": "auditory system disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0024623",
            "name": "otorhinolaryngologic disease"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0001728"
    },
    {
      "id": 3916,
      "label": "active cochlear Meniere disease",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        9300
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:13492",
          "ICD9:386.02",
          "MEDGEN:509990",
          "SCTID:194349005",
          "UMLS:C0155497"
        ],
        "synonyms": [
          "active Meniere's disease, cochlear",
          "active cochlear Meniere's disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0002409",
            "name": "auditory system disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0024623",
            "name": "otorhinolaryngologic disease"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0001729"
    }
  ],
  "roots": [
    {
      "id": 8201,
      "label": "endolymphatic hydrops"
    },
    {
      "id": 18718,
      "label": "hereditary otorhinolaryngologic disease"
    },
    {
      "id": 22991,
      "label": "inherited auditory system disease"
    },
    {
      "id": 24271,
      "label": "hereditary neuromuscular disease"
    }
  ]
}