{
  "id": 10274,
  "label": "Toriello-Carey syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0009021",
  "properties": {
    "xrefs": [
      "GARD:0005225",
      "MEDGEN:163225",
      "MESH:C563127",
      "OMIM:217980",
      "Orphanet:3338",
      "SCTID:722477003",
      "UMLS:C0796184",
      "icd11.foundation:147297969"
    ],
    "synonyms": [
      "Toriello-Carey syndrome",
      "corpus callosum agenesis-blepharophimosis-Robin sequence syndrome",
      "agenesis of corpus callosum with facial anomalies and Robin sequence",
      "corpus callosum agenesis facial anomalies Robin sequence",
      "corpus callosum, agenesis of, with facial anomalies and ROBIN sequence"
    ],
    "definition": "Toriello Carey syndrome is a multiple congenital anomaly syndrome characterized by craniofacial dysmorphic features, cerebral anomalies, swallowing difficulties, cardiac defects and hypotonia."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 16088,
      "label": "multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18951
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0025062",
          "Orphanet:102284"
        ],
        "synonyms": [
          "MCA/variable MR",
          "multiple congenital anomalies-variable intellectual disability with or without dysmorphism syndrome"
        ]
      },
      "child_count": 69,
      "reference_id": "MONDO:0015160"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 16088,
      "label": "multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome"
    }
  ]
}