{
  "id": 9186,
  "label": "autosomal dominant keratitis-ichthyosis-hearing loss syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007850",
  "properties": {
    "xrefs": [
      "DOID:0060871",
      "GARD:0024581",
      "MEDGEN:120536",
      "OMIM:148210",
      "UMLS:C0265336"
    ],
    "synonyms": [
      "KID syndrome, autosomal dominant",
      "keratitis-ichthyosis -deafness syndrome",
      "autosomal dominant keratitis-ichthyosis-deafness syndrome",
      "keratitis-ichthyosis-deafness syndrome, autosomal dominant"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      },
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      }
    ],
    "definition": "Autosomal dominant form of KID syndrome."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 2903,
      "label": "autosomal dominant disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2905
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050736",
          "ICD9:758.5",
          "MEDGEN:539206",
          "SCTID:11164009",
          "UMLS:C0265385"
        ],
        "synonyms": [
          "autosomal dominant disease or disorder",
          "autosomal dominant hereditary disorder",
          "autosomal dominant inherited disorder",
          "disease or disorder, autosomal dominant",
          "disease, autosomal dominant"
        ],
        "definition": "Autosomal dominant form of disease."
      },
      "child_count": 192,
      "reference_id": "MONDO:0000426"
    },
    {
      "id": 18741,
      "label": "KID syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        17917,
        19138
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0003113",
          "ICD9:759.89",
          "MEDGEN:777082",
          "MESH:C536168",
          "MedDRA:10048786",
          "NANDO:1200621",
          "NANDO:2200996",
          "NORD:1326",
          "OMIMPS:148210",
          "Orphanet:477",
          "SCTID:2625009",
          "UMLS:C3665333"
        ],
        "synonyms": [
          "KID/HID syndrome",
          "Keratitis Ichthyosis Deafness Syndrome",
          "Senter syndrome",
          "ichthyosis hystrix Rheydt type",
          "keratitis-ichthyosis-deafness/Hystrix-like ichthyosis-deafness syndrome",
          "keratitis, ichthyosis, and deafness (KID) syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          },
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "Keratitis (and hystrix-like) ichthyosis deafness (KID/HID) syndrome is a rare congenital ectodermal disorder characterized by vascularizing keratitis, hyperkeratotic skin lesions and hearing loss."
      },
      "child_count": 6,
      "reference_id": "MONDO:0018781"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 2903,
      "label": "autosomal dominant disease"
    },
    {
      "id": 18741,
      "label": "KID syndrome"
    }
  ]
}