{
  "id": 18444,
  "label": "neonatal scleroderma",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0018361",
  "properties": {
    "xrefs": [
      "GARD:0021648",
      "MEDGEN:1652107",
      "Orphanet:398127",
      "UMLS:C4509425"
    ],
    "categories": [
      {
        "ref": "MONDO:0003900",
        "name": "connective tissue disorder"
      },
      {
        "ref": "MONDO:0005046",
        "name": "immune system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 18439,
      "label": "secondary neonatal autoimmune disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        8586
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0021643",
          "MEDGEN:1842254",
          "Orphanet:398091",
          "UMLS:C5680041"
        ],
        "synonyms": [
          "Transplacentally acquired neonatal autoimmune disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ]
      },
      "child_count": 6,
      "reference_id": "MONDO:0018356"
    },
    {
      "id": 19180,
      "label": "scleroderma",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7203,
        8586
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:419",
          "EFO:1001993",
          "GARD:0018705",
          "HP:0100324",
          "MEDGEN:3770",
          "MedDRA:10039710",
          "NCIT:C26746",
          "Orphanet:801",
          "UMLS:C0011644"
        ],
        "synonyms": [
          "scleroderma",
          "scleroderma (disease)"
        ],
        "categories": [
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "Scleroderma is a rare autoimmune connective tissue disorder characterized by abnormal hardening of the skin and, sometimes, other organs. It is classified into two main forms: localized scleroderma and systemic sclerosis (SSc), the latter comprising three subsets; diffuse cutaneous SSc (dcSSc), limited cutaneous SSc (lcSSc) and limited SSc (lSSc)."
      },
      "child_count": 6,
      "reference_id": "MONDO:0019340"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 18439,
      "label": "secondary neonatal autoimmune disease"
    },
    {
      "id": 19180,
      "label": "scleroderma"
    }
  ]
}