{
  "id": 23147,
  "label": "palmer pagon syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0043164",
  "properties": {
    "xrefs": [
      "GARD:0004199",
      "MEDGEN:419886",
      "MESH:C538107",
      "Orphanet:2184",
      "UMLS:C2931734"
    ],
    "synonyms": [
      "familial hydrocephalus with a low-insertion umbilicus",
      "hydrocephaly - low insertion umbilicus"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 3395,
      "label": "hydrocephalus",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7209
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:10908",
          "ICD10CM:G91",
          "ICD10WHO:G91",
          "MEDGEN:9335",
          "MESH:D006849",
          "NCIT:C3111",
          "SCTID:230745008",
          "UMLS:C0020255",
          "icd11.foundation:574533444"
        ],
        "synonyms": [
          "hydrocephalus, X-linked",
          "hydrocephalus, nonsyndromic, autosomal recessive"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A disorder characterized by an abnormal increase of cerebrospinal fluid in the ventricles of the brain."
      },
      "child_count": 7,
      "reference_id": "MONDO:0001150"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 3395,
      "label": "hydrocephalus"
    }
  ]
}