{
  "id": 24184,
  "label": "achalasia, familial esophageal",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0100457",
  "properties": {
    "xrefs": [
      "GARD:0000455",
      "MEDGEN:395436",
      "MESH:C536011",
      "OMIM:200400",
      "UMLS:C1860213"
    ],
    "synonyms": [
      "achalasia, familial esophageal"
    ],
    "categories": [
      {
        "ref": "MONDO:0004335",
        "name": "digestive system disorder"
      }
    ],
    "definition": "An instance of achalsia that is caused by an inherited genomic modification in an individual."
  },
  "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": 9971,
      "label": "achalasia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5629
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:9164",
          "HP:0002571",
          "ICD10CM:K22.0",
          "ICD9:530.0",
          "MEDGEN:5023",
          "SCTID:235630008",
          "UMLS:C0014848",
          "icd11.foundation:636464846"
        ],
        "synonyms": [
          "achalasia",
          "achalasia (disease)",
          "achalasia of cardia",
          "achalasia of oesophagus",
          "cardiospasm",
          "esophageal achalasia"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          }
        ],
        "definition": "A finding indicating the lack of adequate relaxation of the lower esophageal sphincter resulting in difficulty swallowing food."
      },
      "child_count": 2,
      "reference_id": "MONDO:0008698"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 5714,
      "label": "hereditary disease"
    },
    {
      "id": 9971,
      "label": "achalasia"
    }
  ]
}