{
  "id": 17596,
  "label": "self-healing collodion baby",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0017267",
  "properties": {
    "xrefs": [
      "GARD:0017303",
      "MEDGEN:383772",
      "MESH:C565473",
      "Orphanet:281122",
      "SCTID:718632004",
      "UMLS:C1855789",
      "icd11.foundation:34721911"
    ],
    "synonyms": [
      "SHCB",
      "SICI",
      "self-improving congenital ichthyosis",
      "self-improving collodion baby"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      }
    ],
    "definition": "Self-healing collodion baby (SHCB) is a minor variant of autosomal recessive congenital ichthyosis (ARCI) characterized by the presence of a collodion membrane at birth that heals within the first weeks of life."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "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": [
    {
      "id": 10668,
      "label": "autosomal recessive congenital ichthyosis 2",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        17596,
        19147
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060710",
          "GARD:0015187",
          "MEDGEN:854762",
          "NCIT:C132827",
          "OMIM:242100",
          "UMLS:C3888093"
        ],
        "synonyms": [
          "ARCI2",
          "autosomal recessive congenital ichthyosis type 2",
          "ichthyosis, congenital, autosomal recessive type 2",
          "NBCIE",
          "NCIE",
          "collodion baby, self-healing",
          "ichthyosiform erythroderma, Brocq congenital, nonbullous form",
          "ichthyosiform erythroderma, Brocq congenital, nonbullous form, formerly",
          "ichthyosiform erythroderma, congenital, nonbullous, 1",
          "ichthyosiform erythroderma, nonbullous congenital, 1",
          "ichthyosiform erythroderma, nonbullous congenital, 1, formerly",
          "ichthyosis, congenital, autosomal recessive 2"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "An autosomal recessive condition caused by mutation(s) in the ALOX12B gene, encoding arachidonate 12-lipoxygenase, 12R-type. It is characterized by dry, thickened, scaly skin."
      },
      "child_count": 0,
      "reference_id": "MONDO:0009439"
    },
    {
      "id": 12770,
      "label": "autosomal recessive congenital ichthyosis 3",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        17596,
        18001,
        19147
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060711",
          "GARD:0015393",
          "MEDGEN:761665",
          "MESH:C564699",
          "OMIM:606545",
          "UMLS:C3539888"
        ],
        "synonyms": [
          "ARCI3",
          "autosomal recessive congenital ichthyosis type 3",
          "ichthyosis, congenital, autosomal recessive type 3",
          "collodion baby, self-healing",
          "ichthyosis, congenital, autosomal recessive 3",
          "ichthyosis, lamellar, 5",
          "ichthyosis, lamellar, 5, formerly"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "Any autosomal recessive congenital ichthyosis in which the cause of the disease is a mutation in the ALOXE3 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0011680"
    }
  ],
  "roots": [
    {
      "id": 17594,
      "label": "autosomal recessive congenital ichthyosis"
    }
  ]
}