{
  "id": 26161,
  "label": "10p13-p14 deletion syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0975905",
  "properties": {
    "xrefs": [
      "GARD:0027416",
      "NCIT:C130982",
      "OMIM:601362",
      "Orphanet:687695"
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 12181,
      "label": "distal monosomy 10p",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        17315
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0001323",
          "MEDGEN:321954",
          "MESH:C563337",
          "Orphanet:1580",
          "SCTID:719686003",
          "UMLS:C1832431"
        ],
        "synonyms": [
          "distal 10p deletion",
          "distal monosomy type 10p",
          "monosomy 10pter",
          "telomeric deletion 10p",
          "10p deletion",
          "10p monosomy",
          "chromosome 10p deletion",
          "deletion 10p",
          "monosomy 10p",
          "partial monosomy 10p"
        ],
        "definition": "Distal monosomy 10p is a rare chromosomal disorder in which the tip of the short arm (p arm) of chromosome 10 is deleted resulting in a variable phenotype depending on the size of the deletion. The deletion may involve only the terminal 10p15 band, or extend towards the centromere to bands 10p14 or 10p13."
      },
      "child_count": 2,
      "reference_id": "MONDO:0011055"
    },
    {
      "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": 12181,
      "label": "distal monosomy 10p"
    },
    {
      "id": 16087,
      "label": "multiple congenital anomalies/dysmorphic syndrome-intellectual disability"
    }
  ]
}