{
  "id": 11922,
  "label": "maternally-inherited diabetes and deafness",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0010785",
  "properties": {
    "xrefs": [
      "GARD:0027358",
      "ICD9:250.80",
      "MEDGEN:90979",
      "MESH:C536246",
      "NCIT:C131859",
      "OMIM:520000",
      "Orphanet:225",
      "SCTID:237619009",
      "UMLS:C0342289",
      "icd11.foundation:2133824111"
    ],
    "synonyms": [
      "MIDD",
      "mitochondrial diabetes",
      "Ballinger Wallace syndrome",
      "Ballinger-Wallace syndrome",
      "Niddm with deafness",
      "diabetes and deafness, maternally inherited",
      "diabetes mellitus type II with deafness",
      "diabetes mellitus, type II, with deafness",
      "diabetes-deafness syndrome, maternally Transmitted",
      "maternally inherited diabetes and deafness",
      "noninsulin-dependent diabetes mellitus with deafness"
    ],
    "categories": [
      {
        "ref": "MONDO:0004335",
        "name": "digestive system disorder"
      },
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ],
    "definition": "Maternally inherited diabetes and deafness (MIDD) is a mitochondrial disorder characterized by maternally transmitted diabetes and sensorineural deafness."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 6752,
      "label": "diabetes mellitus",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4104,
        4915
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:9351",
          "EFO:0000400",
          "HP:0000819",
          "ICD10CM:E08-E13",
          "ICD10WHO:E10-E14",
          "ICD9:250",
          "MEDGEN:8350",
          "MESH:D003920",
          "NANDO:2100157",
          "NANDO:2100158",
          "NCIT:C2985",
          "SCTID:73211009",
          "UMLS:C0011849",
          "icd11.foundation:465177735"
        ],
        "synonyms": [
          "DM",
          "diabetes",
          "diabetes mellitus",
          "diabetes mellitus (disease)"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "A metabolic disorder characterized by abnormally high blood sugar levels due to diminished production of insulin or insulin resistance/desensitization."
      },
      "child_count": 16,
      "reference_id": "MONDO:0005015"
    },
    {
      "id": 16918,
      "label": "mitochondrial oxidative phosphorylation disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5908
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020546",
          "MEDGEN:1825947",
          "Orphanet:223713",
          "UMLS:C5679825",
          "icd11.foundation:1204111545"
        ],
        "synonyms": [
          "OXPHOS disease",
          "OXPHOS system deficiency"
        ],
        "definition": "A multisystem disorder with variable manifestations resulting from a defect in the mitochondrial oxidative phosphorylation (OXPHOS) system."
      },
      "child_count": 48,
      "reference_id": "MONDO:0016387"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 6752,
      "label": "diabetes mellitus"
    },
    {
      "id": 16918,
      "label": "mitochondrial oxidative phosphorylation disorder"
    }
  ]
}