{
  "id": 15515,
  "label": "microcephaly and chorioretinopathy 2",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0014516",
  "properties": {
    "xrefs": [
      "DOID:0080106",
      "GARD:0024997",
      "MEDGEN:863825",
      "OMIM:616171",
      "UMLS:C4015388"
    ],
    "synonyms": [
      "PLK4 microcephaly and chorioretinopathy",
      "microcephaly and chorioretinopathy caused by mutation in PLK4",
      "microcephaly and chorioretinopathy type 2",
      "microcephaly and chorioretinopathy, autosomal recessive, type 2",
      "MCCRP2",
      "microcephaly and chorioretinopathy, autosomal recessive, 2"
    ],
    "categories": [
      {
        "ref": "MONDO:0002022",
        "name": "disorder of orbital region"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      },
      {
        "ref": "MONDO:0024458",
        "name": "disorder of visual system"
      }
    ],
    "definition": "Any microcephaly and chorioretinopathy in which the cause of the disease is a mutation in the PLK4 gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 2760,
      "label": "microcephaly and chorioretinopathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3394,
        6458,
        24226
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0003611",
          "OMIMPS:251270"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 9,
      "reference_id": "MONDO:0000181"
    },
    {
      "id": 7611,
      "label": "autosomal recessive disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2905
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050737",
          "EFO:1000017",
          "ICD9:758.5",
          "MEDGEN:539209",
          "SCTID:85995004",
          "UMLS:C0265388"
        ],
        "synonyms": [
          "autosomal recessive disease or disorder",
          "autosomal recessive hereditary disease",
          "autosomal recessive hereditary disorder",
          "autosomal recessive inherited disease",
          "autosomal recessive inherited disorder",
          "disease or disorder, autosomal recessive",
          "disease, autosomal recessive",
          "recessive hereditary disorder (autosomal)"
        ],
        "definition": "Autosomal recessive form of disease."
      },
      "child_count": 219,
      "reference_id": "MONDO:0006025"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 2760,
      "label": "microcephaly and chorioretinopathy"
    },
    {
      "id": 7611,
      "label": "autosomal recessive disease"
    }
  ]
}