{
  "id": 15994,
  "label": "ichthyosis, congenital, autosomal recessive 12",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0015018",
  "properties": {
    "xrefs": [
      "GARD:0025052",
      "MEDGEN:934588",
      "OMIM:617320",
      "UMLS:C4310621"
    ],
    "synonyms": [
      "ARCI12",
      "ichthyosis, congenital, autosomal recessive 12",
      "ichthyosis, congenital, autosomal recessive 12; ARCI12",
      "ichthyosis, congenital, autosomal recessive type 12"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      }
    ],
    "definition": "Any autosomal recessive congenital ichthyosis in which the cause of the disease is a mutation in the CASP14 gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 17594,
      "label": "autosomal recessive congenital ichthyosis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16624
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060655",
          "GARD:0021106",
          "MEDGEN:697564",
          "NANDO:1200615",
          "NANDO:2200991",
          "OMIMPS:242300",
          "Orphanet:281097",
          "UMLS:C1274215",
          "icd11.foundation:430849255"
        ],
        "synonyms": [
          "ARCI",
          "autosomal recessive inherited ichthyosis",
          "ichthyosis, congenital, autosomal recessive",
          "inherited ichthyosis, autosomal recessive"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "Autosomal recessive form of inherited ichthyosis."
      },
      "child_count": 13,
      "reference_id": "MONDO:0017265"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 17594,
      "label": "autosomal recessive congenital ichthyosis"
    }
  ]
}