{
  "id": 9989,
  "label": "acrogeria",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0008716",
  "properties": {
    "xrefs": [
      "GARD:0006543",
      "ICD9:259.8",
      "MEDGEN:96063",
      "MESH:C538187",
      "NORD:1202",
      "OMIM:201200",
      "Orphanet:2500",
      "SCTID:238872007",
      "UMLS:C0406584",
      "icd11.foundation:1607996977"
    ],
    "synonyms": [
      "Gottron Syndrome",
      "Gottron syndrome",
      "acrogeria, Gottron type",
      "acrometageria",
      "Metageria",
      "familial acrogeria"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      }
    ],
    "definition": "A congenital skin condition characterized by premature aging, more especially in the form of unusually fragile, thin skin on the hands and feet. Its onset is in early childhood; it progresses over the next few years and then remains stable. A bruising tendency has been observed."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 19146,
      "label": "premature aging syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29380
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019017",
          "MEDGEN:65416",
          "MESH:D019588",
          "MedDRA:10063493",
          "Orphanet:79389",
          "UMLS:C0231341"
        ],
        "synonyms": [
          "premature ageing",
          "premature aging"
        ],
        "definition": "Changes in the organism associated with senescence, occurring at an accelerated rate."
      },
      "child_count": 8,
      "reference_id": "MONDO:0019303"
    },
    {
      "id": 23867,
      "label": "hereditary skin disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        6820
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MESH:D012873",
          "SCTID:239001006"
        ],
        "synonyms": [
          "disease, genetic skin",
          "diseases, genetic skin",
          "genetic skin disease",
          "genetic skin diseases",
          "genodermatosis",
          "skin disease, genetic"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "An instance of skin disease that is caused by a modification of the individual's genome."
      },
      "child_count": 228,
      "reference_id": "MONDO:0100118"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 19146,
      "label": "premature aging syndrome"
    },
    {
      "id": 23867,
      "label": "hereditary skin disorder"
    }
  ]
}