{
  "id": 13667,
  "label": "deafness-infertility syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0012621",
  "properties": {
    "xrefs": [
      "GARD:0011911",
      "ICD9:758.39",
      "MEDGEN:370197",
      "MESH:C567010",
      "OMIM:611102",
      "Orphanet:94064",
      "SCTID:700489002",
      "UMLS:C1970187",
      "icd11.foundation:1430704280"
    ],
    "synonyms": [
      "DIS",
      "deafness and male infertility",
      "deafness-infertility syndrome",
      "dis",
      "chromosome 15Q15.3 deletion syndrome",
      "deafness, sensorineural, and Male infertility",
      "sensorineural deafness and male infertility"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      }
    ],
    "definition": "Deafness-infertility syndrome (DIS) is a very rare syndrome associating sensorineural deafness and male infertility."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 4370,
      "label": "syndromic disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29379
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:225",
          "MEDGEN:11688",
          "MESH:D013577",
          "NCIT:C28193",
          "OGMS:0000086",
          "UMLS:C0039082"
        ],
        "synonyms": [
          "cluster, symptom",
          "clusters, symptom",
          "symptom cluster",
          "symptom clusters",
          "syndrome",
          "syndrome associated with disease or disorder",
          "syndromes",
          "syndromic disease",
          "syndromic disease or disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "A group of signs, symptoms, and clinicopathological characteristics that may or may not have a genetic basis and collectively define an abnormal condition."
      },
      "child_count": 1182,
      "reference_id": "MONDO:0002254"
    },
    {
      "id": 17332,
      "label": "partial deletion of the long arm of chromosome 15",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3128
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:444123",
          "MESH:C538038",
          "Orphanet:262119",
          "UMLS:C2931708"
        ],
        "synonyms": [
          "partial deletion of chromosome 15q",
          "partial deletion of the long arm of chromosome type 15",
          "partial monosomy of chromosome 15q",
          "partial monosomy of the long arm of chromosome 15",
          "15q deletion",
          "15q monosomy",
          "chromosome 15q deletion",
          "deletion 15q",
          "monosomy 15q",
          "partial monosomy 15q"
        ]
      },
      "child_count": 9,
      "reference_id": "MONDO:0016913"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 4370,
      "label": "syndromic disease"
    },
    {
      "id": 17332,
      "label": "partial deletion of the long arm of chromosome 15"
    }
  ]
}