{
  "id": 8795,
  "label": "Cri-du-chat syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007404",
  "properties": {
    "xrefs": [
      "DECIPHER:2",
      "DOID:12580",
      "GARD:0006213",
      "ICD9:758.31",
      "ICD9:758.39",
      "MEDGEN:41345",
      "MESH:D003410",
      "MedDRA:10011385",
      "NANDO:1200684",
      "NANDO:2200961",
      "NCIT:C34518",
      "NORD:1015",
      "OMIM:123450",
      "Orphanet:281",
      "SCTID:70173007",
      "UMLS:C0010314",
      "icd11.foundation:620584190"
    ],
    "synonyms": [
      "5p deletion syndrome",
      "5p partial monosomy syndrome",
      "Cat-Cry syndrome",
      "Cri du Chat Syndrome",
      "Cri du chat syndrome",
      "Cri-du-chat syndrome",
      "chromosome 5p deletion syndrome",
      "deletion 5p",
      "monosomy type 5p",
      "5p minus syndrome",
      "5p- syndrome",
      "Cat Cry syndrome",
      "chromosome 5P deletion syndrome",
      "chromosome 5p- syndrome",
      "monosomy 5p"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      }
    ],
    "definition": "Monosomy 5p, also known as Cri du chat syndrome, is a rare autosomal deletion syndrome characterized by a mewing cry (cri du chat) in infancy, multiple congenital anomalies, intellectual disability, microcephaly, and facial dysmorphism."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 4370,
      "label": "syndromic disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29379
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:225",
          "MEDGEN:11688",
          "MESH:D013577",
          "NCIT:C28193",
          "OGMS:0000086",
          "UMLS:C0039082"
        ],
        "synonyms": [
          "cluster, symptom",
          "clusters, symptom",
          "symptom cluster",
          "symptom clusters",
          "syndrome",
          "syndrome associated with disease or disorder",
          "syndromes",
          "syndromic disease",
          "syndromic disease or disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "A group of signs, symptoms, and clinicopathological characteristics that may or may not have a genetic basis and collectively define an abnormal condition."
      },
      "child_count": 1182,
      "reference_id": "MONDO:0002254"
    },
    {
      "id": 17311,
      "label": "partial deletion of the short arm of chromosome 5",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        17295
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:1788277",
          "Orphanet:261893",
          "UMLS:C5547451",
          "icd11.foundation:1109271336"
        ],
        "synonyms": [
          "partial deletion of chromosome 5p",
          "partial deletion of the short arm of chromosome type 5",
          "partial monosomy of chromosome 5p",
          "partial monosomy of the short arm of chromosome 5"
        ]
      },
      "child_count": 1,
      "reference_id": "MONDO:0016887"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 4370,
      "label": "syndromic disease"
    },
    {
      "id": 17311,
      "label": "partial deletion of the short arm of chromosome 5"
    }
  ]
}