{
  "id": 15020,
  "label": "autosomal recessive congenital ichthyosis 9",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0014010",
  "properties": {
    "xrefs": [
      "DOID:0060718",
      "GARD:0015896",
      "MEDGEN:767263",
      "OMIM:615023",
      "UMLS:C3554349"
    ],
    "synonyms": [
      "ARCI9",
      "autosomal recessive congenital ichthyosis 9",
      "autosomal recessive congenital ichthyosis type 9",
      "ichthyosis, congenital, autosomal recessive type 9",
      "ichthyosis, congenital, autosomal recessive 9"
    ],
    "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 CERS3 gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 19147,
      "label": "congenital non-bullous ichthyosiform erythroderma",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7611,
        17594
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:1699",
          "GARD:0009736",
          "HP:0007431",
          "MEDGEN:38180",
          "NANDO:1200616",
          "NANDO:1200617",
          "Orphanet:79394",
          "SCTID:205550003",
          "UMLS:C0079154",
          "icd11.foundation:546439698"
        ],
        "synonyms": [
          "CIE",
          "alligator skin",
          "congenital ichthyosiform erythroderma",
          "congenital ichthyosiform erythroderma (disease)",
          "congenital non bullous ichthyosiform erythroderma",
          "erythrodermic ichthyosis",
          "ichthyosiform erythroderma",
          "non-bullous congenital ichthyosiform erythroderma",
          "nonbullous congenital ichthyosiform erythroderma",
          "lamellar desquamation of the newborn",
          "lamellar ichthyosis"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "A variant of autosomal recessive congenital ichthyosis (ARCI), a rare epidermal disease, characterized by fine, whitish scales on a background of erythematous skin over the whole body."
      },
      "child_count": 12,
      "reference_id": "MONDO:0019306"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 19147,
      "label": "congenital non-bullous ichthyosiform erythroderma"
    }
  ]
}