{
  "id": 12024,
  "label": "acrocardiofacial syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0010890",
  "properties": {
    "xrefs": [
      "DOID:0070419",
      "GARD:0001167",
      "MEDGEN:324947",
      "MESH:C563936",
      "OMIM:600460",
      "Orphanet:2008",
      "UMLS:C1838121",
      "icd11.foundation:976844546"
    ],
    "synonyms": [
      "ACFS",
      "CCGE syndrome",
      "acrocardiofacial syndrome",
      "cleft palate-cardiac defect-genital anomalies-ectrodactyly syndrome",
      "CCGE",
      "cleft palate, CARDIAC defect, genital anomalies, and ectrodactyly"
    ],
    "definition": "Acro-cardio-facial syndrome (ACFS) is a rare genetic disorder characterized by split-hand/split-foot malformation (SHFM), facial anomalies, cleft lip/palate, congenital heart defect (CHD), genital anomalies, and intellectual deficit."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 16087,
      "label": "multiple congenital anomalies/dysmorphic syndrome-intellectual disability",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18951
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019832",
          "MEDGEN:1826158",
          "Orphanet:102283",
          "UMLS:C5680372"
        ],
        "synonyms": [
          "MCA/MR",
          "multiple congenital anomalies-intellectual disability with or without dysmorphism",
          "multiple congenital anomalies/dysmorphic syndrome-intellectual disability"
        ]
      },
      "child_count": 338,
      "reference_id": "MONDO:0015159"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 16087,
      "label": "multiple congenital anomalies/dysmorphic syndrome-intellectual disability"
    }
  ]
}