{
  "id": 18650,
  "label": "19p13.3 microduplication syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0018658",
  "properties": {
    "xrefs": [
      "GARD:0021875",
      "MEDGEN:1807189",
      "Orphanet:447980",
      "UMLS:C5679996"
    ],
    "synonyms": [
      "dup(19)(p13.13)"
    ],
    "definition": "19p13.3 microduplication syndrome is a rare, genetic, syndromic intellectual disability characterized by intrauterine growth retardation, microcephaly, hypotonia, motor and neurodevelopmental delay, speech delay, intellectual disability, and mild dysmorphic features."
  },
  "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"
    },
    {
      "id": 18651,
      "label": "partial duplication of the short arm of chromosome 19",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        17353
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:1380854",
          "Orphanet:447985",
          "UMLS:C4518508"
        ],
        "synonyms": [
          "partial duplication of chromosome 19p",
          "partial duplication of the short arm of chromosome type 19",
          "partial trisomy of chromosome 19p",
          "partial trisomy of the short arm of chromosome 19"
        ]
      },
      "child_count": 1,
      "reference_id": "MONDO:0018659"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 16087,
      "label": "multiple congenital anomalies/dysmorphic syndrome-intellectual disability"
    },
    {
      "id": 18651,
      "label": "partial duplication of the short arm of chromosome 19"
    }
  ]
}