{
  "id": 19651,
  "label": "Leydig cell hypoplasia due to partial LH resistance",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0019931",
  "properties": {
    "xrefs": [
      "DOID:0112261",
      "GARD:0016852",
      "MEDGEN:1739565",
      "Orphanet:96266",
      "UMLS:C5438975"
    ],
    "synonyms": [
      "46,XY DSD due to partial LH receptor inactivation",
      "46,XY DSD due to partial LH resistance",
      "46,XY DSD due to partial luteinizing hormone resistance",
      "Leydig cell hypoplasia due to partial LH receptor inactivation",
      "Leydig cell hypoplasia due to partial luteinizing hormone receptor inactivation",
      "Leydig cell hypoplasia due to partial luteinizing hormone resistance"
    ],
    "categories": [
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 10616,
      "label": "Leydig cell hypoplasia, type 1",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        19032
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0024669",
          "MEDGEN:120576",
          "OMIM:238320",
          "UMLS:C0266432"
        ],
        "synonyms": [
          "LHCGR Leydig cell hypoplasia",
          "Leydig cell hypoplasia caused by mutation in LHCGR",
          "leydig cell hypoplasia with hypergonadotropic hypogonadism",
          "leydig cell hypoplasia with pseudohermaphroditism",
          "Leydig cell Hypoplasia, type 2",
          "Leydig cell agenesis",
          "Leydig cell hypoplasia with male pseudohermaphroditism",
          "Leydig cell hypoplasia, complete",
          "Leydig cell hypoplasia, partial",
          "Leydig cell hypoplasia, type I",
          "hypergonadotropic hypogonadism, Male, due to Lhcgr defect",
          "luteinizing hormone resistance, female"
        ],
        "categories": [
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "Any Leydig cell hypoplasia in which the cause of the disease is a mutation in the LHCGR gene."
      },
      "child_count": 4,
      "reference_id": "MONDO:0009384"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 10616,
      "label": "Leydig cell hypoplasia, type 1"
    }
  ]
}