{
  "id": 7109,
  "label": "visceral leishmaniasis",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0005445",
  "properties": {
    "xrefs": [
      "DOID:9146",
      "EFO:0005045",
      "GARD:0024188",
      "ICD10CM:B55.0",
      "ICD9:085.0",
      "MEDGEN:44098",
      "MESH:D007898",
      "NCIT:C34771",
      "OMIMPS:608207",
      "SCTID:186803007",
      "UMLS:C0023290",
      "icd11.foundation:1646564717"
    ],
    "synonyms": [
      "kala-azar",
      "viscus leishmaniasis",
      "kala-azar susceptibility",
      "kala-azar, susceptibility to"
    ],
    "definition": "A severe form of leishmaniasis characterized by irregular bouts of fever, substantial weight loss, swelling of the spleen and liver, and anemia (which may be serious). If left untreated it may lead to death. Two species of Leishmania are known to give rise to the visceral form of the disease. The species commonly found in East Africa and the Indian subcontinent is L. donovani and the species found in Europe, North Africa, and Latin America is L. infantum, also known as L. chagasi."
  },
  "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": 13060,
      "label": "leishmaniasis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4516,
        23869
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:9065",
          "EFO:0005044",
          "GARD:0006881",
          "ICD10CM:B55",
          "ICD10WHO:B55",
          "ICD9:085",
          "ICD9:085.9",
          "MEDGEN:9714",
          "MESH:D007896",
          "MedDRA:10024198",
          "NCIT:C34767",
          "NORD:1895",
          "Orphanet:507",
          "SCTID:80612004",
          "UMLS:C0023281",
          "icd11.foundation:1082373067"
        ],
        "synonyms": [
          "cutaneous leishmaniasis (subtype)",
          "visceral leishmaniasis (subtype)"
        ],
        "definition": "Infectious disease that is transmitted through the bite of hematophagous female phlebotomine sand flies. The clinical spectrum ranges from asymptomatic to clinically overt disease which can remain localized to the skin or disseminate to the upper oral and respiratory mucous membranes or throughout the reticulo-endothelial system. Three main clinical syndromes have been described: visceral (or Kala-Azar; with fever, weight loss, hepatosplenomegaly), cutaneous, and mucocutaneous leishmaniasis (cutaneous or mucocutaneous ulceration)."
      },
      "child_count": 6,
      "reference_id": "MONDO:0011989"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 5714,
      "label": "hereditary disease"
    },
    {
      "id": 13060,
      "label": "leishmaniasis"
    }
  ]
}