{
  "id": 10305,
  "label": "autosomal recessive cutis laxa type 2, classic type",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0009054",
  "properties": {
    "xrefs": [
      "DOID:0070141",
      "GARD:0017546",
      "MEDGEN:1825992",
      "MESH:C562632",
      "Orphanet:357074",
      "SCTID:73856006",
      "UMLS:C5679922"
    ],
    "synonyms": [
      "ARCL2, Debré type",
      "ARCL2, classic type",
      "autosomal recessive cutis laxa type 2, Debre type",
      "autosomal recessive cutis laxa type 2, Debré type",
      "ARCL2A",
      "Arcl2",
      "autosomal recessive cutis laxa type II classic type"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 23977,
      "label": "inherited cutis laxa",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        16769
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0026092",
          "MEDGEN:609465",
          "OMIMPS:123700",
          "UMLS:C0432334"
        ],
        "synonyms": [
          "hereditary cutis laxa"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "An instance of cutis laxa that is inherited."
      },
      "child_count": 28,
      "reference_id": "MONDO:0100237"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 23977,
      "label": "inherited cutis laxa"
    }
  ]
}