{
  "id": 9609,
  "label": "familial male-limited precocious puberty",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0008303",
  "properties": {
    "xrefs": [
      "DOID:0111545",
      "GARD:0004475",
      "MEDGEN:87444",
      "MedDRA:10063654",
      "MedDRA:10063656",
      "OMIM:176410",
      "Orphanet:3000",
      "SCTID:237818003",
      "UMLS:C0342549"
    ],
    "synonyms": [
      "pubertas praecox",
      "FMPP",
      "LHCGR peripheral precocious puberty",
      "familial gonadotropin-independent male-limited sexual precocity",
      "leydig cell adenoma, somatic, with precocious puberty",
      "male-limited precocious puberty",
      "peripheral precocious puberty caused by mutation in LHCGR",
      "precocious puberty, male",
      "testotoxicosis",
      "testotoxicosis, familial",
      "Leydig cell adenoma, somatic, with male-limited precocious puberty",
      "familial Testotoxicosis (subtype)",
      "precocious puberty, male limited",
      "precocious puberty, male-limited",
      "sexual precocity, familial, gonadotropin-independent"
    ],
    "categories": [
      {
        "ref": "MONDO:0005039",
        "name": "reproductive system disorder"
      },
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ],
    "definition": "Familial male limited precocious puberty (FMPP) is a gonadotropin-independent familial form of male-limited precocious puberty, generally presenting between 2-5 years of age as accelerated growth, early development of secondary sexual characteristics and reduced adult height."
  },
  "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": 16544,
      "label": "peripheral precocious puberty",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2721
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020141",
          "MEDGEN:1842596",
          "NANDO:2200378",
          "Orphanet:178040",
          "SCTID:736606009",
          "UMLS:C5680513",
          "icd11.foundation:1495024153"
        ],
        "synonyms": [
          "GIPP",
          "gonadotropin independent precocious puberty",
          "gonadotropin-independent precocious puberty",
          "precocious pseudopuberty"
        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "Precocious puberty caused by sex hormones."
      },
      "child_count": 1,
      "reference_id": "MONDO:0015791"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 5714,
      "label": "hereditary disease"
    },
    {
      "id": 16544,
      "label": "peripheral precocious puberty"
    }
  ]
}