{
  "id": 9142,
  "label": "hypoparathyroidism-deafness-renal disease syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007797",
  "properties": {
    "xrefs": [
      "DOID:0060878",
      "GARD:0002911",
      "MEDGEN:374443",
      "MESH:C537907",
      "NCIT:C130983",
      "NORD:837",
      "OMIM:146255",
      "Orphanet:2237",
      "SCTID:724282009",
      "UMLS:C1840333"
    ],
    "synonyms": [
      "Barakat Syndrome",
      "Barakat syndrome",
      "HDR syndrome",
      "hypoparathyroidism, deafness, and renal anomalies syndrome",
      "hypoparathyroidism, sensorineural deafness, and renal disease",
      "hypoparathyroidism-deafness-renal disease syndrome",
      "HDR",
      "hypoparathyroidism, sensorineural deafness, and renal dysplasia",
      "hypoparathyroidism, sensorineural deafness, and renal dysplasia syndrome",
      "nephrosis, nerve deafness, and hypoparathyroidism"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      }
    ],
    "definition": "The HDR syndrome is an inherited condition consisting of hypoparathyroidism, sensorineural deafness and renal disease."
  },
  "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": 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": 17315,
      "label": "partial deletion of the short arm of chromosome 10",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        17300
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:162776",
          "Orphanet:261938",
          "UMLS:C0795836",
          "icd11.foundation:350543001"
        ],
        "synonyms": [
          "partial deletion of chromosome 10p",
          "partial deletion of the short arm of chromosome type 10",
          "partial monosomy of chromosome 10p",
          "partial monosomy of the short arm of chromosome 10"
        ]
      },
      "child_count": 4,
      "reference_id": "MONDO:0016892"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 4370,
      "label": "syndromic disease"
    },
    {
      "id": 5714,
      "label": "hereditary disease"
    },
    {
      "id": 17315,
      "label": "partial deletion of the short arm of chromosome 10"
    }
  ]
}