{
  "id": 19925,
  "label": "monosomy X",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0020466",
  "properties": {
    "xrefs": [
      "GARD:0019676",
      "MEDGEN:116607",
      "NCIT:C36630",
      "Orphanet:99226",
      "SCTID:710008008",
      "UMLS:C0242526",
      "icd11.foundation:95979116"
    ],
    "synonyms": [
      "monosomy type X"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0005039",
        "name": "reproductive system disorder"
      },
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ]
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 1,
  "parents": [
    {
      "id": 19317,
      "label": "Turner syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4130,
        4370,
        18156,
        19578
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:3491",
          "GARD:0007831",
          "ICD10CM:Q96.0",
          "ICD10WHO:Q96",
          "ICD9:758.7",
          "MEDGEN:21734",
          "MESH:D014424",
          "MedDRA:10045181",
          "NANDO:2200410",
          "NCIT:C26900",
          "NORD:1806",
          "Orphanet:881",
          "SCTID:38804009",
          "UMLS:C0041408",
          "icd11.foundation:1987089698"
        ],
        "synonyms": [
          "gonadal dysgenesis",
          "45,X gonadal dysgenesis",
          "45,X syndrome",
          "45,X/46,XX syndrome",
          "45,X0 syndrome",
          "45X syndrome",
          "karyotype 45, X",
          "monosomy X",
          "45, X syndrome",
          "Bonnevie-Ullrich syndrome",
          "Schereshevkii Turner syndrome",
          "Turner Varny syndrome",
          "Ullrich-Turner syndrome",
          "chromosome X monosomy X",
          "genital dwarfism",
          "genital dwarfism, Turner type",
          "gonadal dysgenesis (45,X)",
          "gonadal dysgenesis Turner type"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "Turner syndrome is a chromosomal disorder associated with the complete or partial absence of an X chromosome."
      },
      "child_count": 12,
      "reference_id": "MONDO:0019499"
    },
    {
      "id": 20054,
      "label": "monosomy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        24460
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:6432",
          "MESH:D009006",
          "NCIT:C3239",
          "UMLS:C0026499"
        ],
        "definition": "A chromosomal abnormality consisting of the absence of one chromosome from the normal diploid number."
      },
      "child_count": 4,
      "reference_id": "MONDO:0020639"
    },
    {
      "id": 24425,
      "label": "chromosome X disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19717
      ],
      "type_id": 0,
      "properties": {
        "definition": "Chromosomal disorder in which chromosome X is affected."
      },
      "child_count": 13,
      "reference_id": "MONDO:0700027"
    }
  ],
  "children": [
    {
      "id": 19926,
      "label": "mosaic monosomy X",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19925
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019677",
          "MEDGEN:873772",
          "Orphanet:99228",
          "SCTID:710010005",
          "UMLS:C4040907"
        ],
        "synonyms": [
          "Mosaic Turner syndrome",
          "Mosaic monosomy type X",
          "XX/XO"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0020467"
    }
  ],
  "roots": [
    {
      "id": 19317,
      "label": "Turner syndrome"
    },
    {
      "id": 20054,
      "label": "monosomy"
    },
    {
      "id": 24425,
      "label": "chromosome X disorder"
    }
  ]
}