{
  "id": 10978,
  "label": "oculodentodigital dysplasia, autosomal recessive",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0009768",
  "properties": {
    "xrefs": [
      "GARD:0015213",
      "MEDGEN:412708",
      "MESH:C567605",
      "OMIM:257850",
      "UMLS:C2749477"
    ],
    "synonyms": [
      "autosomal recessive oculodentodigital dysplasia",
      "oculodentodigital dysplasia, autosomal recessive",
      "ODDD, autosomal recessive",
      "ODOD recessive",
      "ODOD, autosomal recessive",
      "oculodentoosseous dysplasia recessive",
      "oculodentoosseous dysplasia, autosomal recessive"
    ],
    "categories": [
      {
        "ref": "MONDO:0002022",
        "name": "disorder of orbital region"
      },
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      },
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0024458",
        "name": "disorder of visual system"
      }
    ],
    "definition": "Autosomal recessive form of oculodentodigital dysplasia."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "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"
    },
    {
      "id": 9428,
      "label": "oculodentodigital dysplasia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7019,
        16088,
        18360,
        19138
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060291",
          "GARD:0007239",
          "ICD9:759.89",
          "MEDGEN:167236",
          "MESH:C563160",
          "MedDRA:10063691",
          "NORD:1519",
          "OMIM:164200",
          "Orphanet:2710",
          "SCTID:38215007",
          "UMLS:C0812437"
        ],
        "synonyms": [
          "Meyer-Schwickerath syndrome",
          "ODDD syndrome",
          "Oculo-Dento-Digital Dysplasia",
          "oculo-dento-digital dysplasia",
          "oculodentodigital dysplasia",
          "oculodentoosseous dysplasia",
          "odd syndrome",
          "ODDD",
          "oculo-dento-digital syndrome",
          "oculodentodigital syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          },
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "Oculodentodigital dysplasia (ODDD) is characterized by craniofacial, neurologic, limb and ocular abnormalities."
      },
      "child_count": 4,
      "reference_id": "MONDO:0008111"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 7611,
      "label": "autosomal recessive disease"
    },
    {
      "id": 9428,
      "label": "oculodentodigital dysplasia"
    }
  ]
}