{
  "id": 9081,
  "label": "acne inversa, familial, 1",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007728",
  "properties": {
    "xrefs": [
      "MEDGEN:1631104",
      "OMIM:142690",
      "UMLS:C4551962"
    ],
    "synonyms": [
      "NCSTN familial acne inversa",
      "acne inversa, familial, 1",
      "acne inversa, familial, type 1",
      "familial acne inversa caused by mutation in NCSTN",
      "ACNINV1",
      "acne inversa, familial",
      "hidradenitis suppurativa, familial"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      }
    ],
    "definition": "Any familial acne inversa in which the cause of the disease is a mutation in the NCSTN gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 21462,
      "label": "familial acne inversa",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        8042,
        23867
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:326766",
          "OMIMPS:142690",
          "UMLS:C1840560"
        ],
        "synonyms": [
          "ACNINV",
          "familial hidradenitis suppurativa",
          "hereditary hidradenitis suppurativa"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "An instance of hidradenitis suppurativa that is caused by an inherited modification of the individual's genome."
      },
      "child_count": 6,
      "reference_id": "MONDO:0024516"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 21462,
      "label": "familial acne inversa"
    }
  ]
}