{
  "id": 10114,
  "label": "atrichia with papular lesions",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0008847",
  "properties": {
    "xrefs": [
      "DOID:0060689",
      "GARD:0016762",
      "MEDGEN:395299",
      "MESH:C565924",
      "OMIM:209500",
      "Orphanet:86819",
      "SCTID:715963002",
      "UMLS:C1859592"
    ],
    "synonyms": [
      "atrichia with papular lesions",
      "papular atrichia",
      "APL"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      }
    ],
    "definition": "Atrichia with papular lesions is a rare inherited form of alopecia characterized by irreversible hair loss during the neonatal period on all hear-bearing areas of the body, later associated with the development of papular lesions all over the body and preferentially on the face and extensor surfaces of the extremities."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 5714,
      "label": "hereditary disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29382
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:630",
          "EFO:0000508",
          "ICD9:799.89",
          "MEDGEN:5527",
          "MESH:D030342",
          "NCIT:C3101",
          "SCTID:32895009",
          "UMLS:C0019247"
        ],
        "synonyms": [
          "genetic condition",
          "genetic disease",
          "genetic disorder",
          "hereditary disease",
          "hereditary disease or disorder",
          "hereditary diseases",
          "inherited disease",
          "inherited genetic disease",
          "molecular disease",
          "Mendelian disease",
          "familial disorder",
          "inborn disorder"
        ],
        "definition": "A disease that is caused by genetic modifications where those modifications are inherited from a parent's genome."
      },
      "child_count": 1925,
      "reference_id": "MONDO:0003847"
    },
    {
      "id": 6660,
      "label": "alopecia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19134
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:987",
          "ICD9:704.0",
          "ICD9:704.00",
          "ICD9:704.09",
          "MEDGEN:7982",
          "MESH:D000505",
          "NCIT:C50575",
          "Orphanet:79364",
          "SCTID:56317004",
          "UMLS:C0002170",
          "icd11.foundation:1313926062"
        ],
        "synonyms": [
          "alopecia",
          "hair loss",
          "loss Of hair",
          "alopecia areata"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "Hair loss usually from the scalp. It may result in bald spots or spread to the entire scalp or the entire epidermis. It may be androgenetic or caused by chemotherapeutic agents, compulsive hair pulling, autoimmune disorders or congenital conditions."
      },
      "child_count": 26,
      "reference_id": "MONDO:0004907"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 5714,
      "label": "hereditary disease"
    },
    {
      "id": 6660,
      "label": "alopecia"
    }
  ]
}