{
  "id": 17108,
  "label": "acquired deficiency anemia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0016625",
  "properties": {
    "xrefs": [
      "MEDGEN:1842907",
      "Orphanet:248302",
      "UMLS:C5680693"
    ],
    "synonyms": [
      "rare acquired deficiency anaemia",
      "rare acquired deficiency anemia"
    ],
    "categories": [
      {
        "ref": "MONDO:0005570",
        "name": "hematologic disorder"
      }
    ],
    "definition": "An instance of deficiency anemia that is acquired during the lifetime of the individual."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 1,
  "parents": [
    {
      "id": 3835,
      "label": "deficiency anemia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4394
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:13121",
          "GARD:0022980",
          "ICD9:281.8",
          "ICD9:281.9",
          "MEDGEN:508256",
          "SCTID:267513007",
          "UMLS:C0041782"
        ],
        "synonyms": [
          "deficiency anemias",
          "unspecified deficiency anaemia",
          "unspecified deficiency anemia"
        ],
        "categories": [
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ]
      },
      "child_count": 3,
      "reference_id": "MONDO:0001639"
    }
  ],
  "children": [
    {
      "id": 18823,
      "label": "Plummer-Vinson syndrome",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        4370,
        17108
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0008259",
          "ICD10CM:D50.1",
          "ICD9:280.8",
          "MEDGEN:45967",
          "MESH:D011004",
          "MedDRA:10040664",
          "NCIT:C85016",
          "Orphanet:54028",
          "SCTID:80126007",
          "UMLS:C0032249",
          "icd11.foundation:1568337509"
        ],
        "synonyms": [
          "Kelly-Paterson syndrome",
          "Sideropenic dysphagia",
          "Kelly's syndrome",
          "Paterson's syndrome",
          "Paterson-Brown-Kelly syndrome",
          "Paterson-Kelly syndrome",
          "Paterson’s syndrome",
          "Plummer Vinson syndrome",
          "dysphagia sideropenica"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "Plummer-Vinson or Paterson-Kelly syndrome presents as a classical triad of dysphagia, iron-deficiency anemia and esophageal webs."
      },
      "child_count": 0,
      "reference_id": "MONDO:0018895"
    }
  ],
  "roots": [
    {
      "id": 3835,
      "label": "deficiency anemia"
    }
  ]
}