{
  "id": 10321,
  "label": "Dandy-Walker syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0009072",
  "properties": {
    "xrefs": [
      "DOID:2785",
      "EFO:1000890",
      "GARD:0006242",
      "MEDGEN:4150",
      "MESH:D003616",
      "MedDRA:10048411",
      "NANDO:2200821",
      "NCIT:C75012",
      "NORD:1032",
      "OMIM:220200",
      "Orphanet:217",
      "SCTID:14447001",
      "UMLS:C0010964",
      "icd11.foundation:993088960"
    ],
    "synonyms": [
      "Dandy Walker Malformation",
      "Dandy-Walker syndrome",
      "Dandy-Walker syndrome, Isolated cases",
      "DW complex",
      "DWS",
      "Dandy-Walker complex",
      "Dandy-Walker malformation",
      "Dandy-Walker syndrome or malformation (type of DW complex)",
      "Dandy-Walker variant (type of DW complex)",
      "isolated Dandy-Walker malformation",
      "mega cisterna magna (type of DW complex)"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Dandy-Walker malformation (DWM) is the association of three signs: hydrocephalus, partial or complete absence of the cerebellar vermis, and posterior fossa cyst contiguous with the fourth ventricle, presenting early in life with hydrocephalus, bulging occiput and posterior fossa signs such as cranial nerve palsies, nystagmus and ataxia."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 3,
  "parents": [
    {
      "id": 4515,
      "label": "cerebellar disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7209
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:2786",
          "MEDGEN:40186",
          "MESH:D002526",
          "SCTID:223176004",
          "UMLS:C0007760"
        ],
        "synonyms": [
          "cerebellum disease",
          "cerebellum disease or disorder",
          "disease of cerebellum",
          "disease or disorder of cerebellum",
          "disorder of cerebellum"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Diseases that affect the structure or function of the cerebellum. Cardinal manifestations of cerebellar dysfunction include dysmetria, gait ataxia, and muscle hypotonia."
      },
      "child_count": 5,
      "reference_id": "MONDO:0002427"
    },
    {
      "id": 19751,
      "label": "cystic malformation of the posterior fossa",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19709
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0025153",
          "ICD9:742.4",
          "MEDGEN:783289",
          "Orphanet:98520",
          "SCTID:35111000119109",
          "UMLS:C3662134"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 4,
      "reference_id": "MONDO:0020134"
    }
  ],
  "children": [
    {
      "id": 17485,
      "label": "isolated Dandy-Walker malformation with hydrocephalus",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        10321
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020993",
          "MEDGEN:1842616",
          "Orphanet:269212",
          "UMLS:C5680779"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0017110"
    },
    {
      "id": 17486,
      "label": "isolated Dandy-Walker malformation without hydrocephalus",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        10321
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020994",
          "MEDGEN:1842486",
          "Orphanet:269215",
          "UMLS:C5680778"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0017111"
    },
    {
      "id": 21058,
      "label": "Dandy-Walker malformation with nasopharyngeal teratoma and diaphragmatic hernia",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        10321
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0000137",
          "MEDGEN:419910",
          "MESH:C538340",
          "UMLS:C2931823"
        ],
        "synonyms": [
          "Aughton sloan Milad syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0022930"
    }
  ],
  "roots": [
    {
      "id": 4515,
      "label": "cerebellar disorder"
    },
    {
      "id": 19751,
      "label": "cystic malformation of the posterior fossa"
    }
  ]
}