{
  "id": 20811,
  "label": "calloso-genital dysplasia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0022060",
  "properties": {
    "xrefs": [
      "GARD:0027362",
      "MEDGEN:419867",
      "MESH:C537962",
      "UMLS:C2931677"
    ],
    "synonyms": [
      "primary amenorrhoea with coloboma and total agenesis of the corpus callosum"
    ],
    "categories": [
      {
        "ref": "MONDO:0002022",
        "name": "disorder of orbital region"
      },
      {
        "ref": "MONDO:0005039",
        "name": "reproductive system disorder"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      },
      {
        "ref": "MONDO:0024458",
        "name": "disorder of visual system"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 3690,
      "label": "coloboma",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7019
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:12270",
          "ICD9:743.49",
          "MEDGEN:1046",
          "MESH:D003103",
          "NCIT:C98877",
          "Orphanet:194",
          "SCTID:93390002",
          "UMLS:C0009363"
        ],
        "synonyms": [
          "coloboma of the eye",
          "ocular coloboma",
          "coloboma of macula",
          "congenital ocular coloboma"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "An abnormality in which a part of a structure in one or both eyes is missing."
      },
      "child_count": 8,
      "reference_id": "MONDO:0001476"
    },
    {
      "id": 4016,
      "label": "amenorrhea",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29362
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:13938",
          "HP:0000141",
          "ICD9:626.0",
          "MEDGEN:8016",
          "MESH:D000568",
          "NCIT:C61443",
          "UMLS:C0002453"
        ],
        "synonyms": [
          "absence of menstruation",
          "amenorrhea",
          "amenorrhea (disease)"
        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          }
        ],
        "definition": "The absence of menses in a woman who has achieved reproductive age."
      },
      "child_count": 3,
      "reference_id": "MONDO:0001836"
    },
    {
      "id": 10275,
      "label": "corpus callosum, agenesis of",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4427,
        24270
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0027261",
          "MEDGEN:104498",
          "MESH:D061085",
          "NCIT:C98905",
          "OMIM:217990",
          "Orphanet:200",
          "SCTID:5102002",
          "UMLS:C0175754"
        ],
        "synonyms": [
          "agenesis of corpus callosum",
          "corpus callosum agenesis",
          "corpus callosum, agenesis of",
          "ACC",
          "agenesis of the corpus callosum",
          "isolated corpus callosum agenesis"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A congenital abnormality characterized by the complete absence of the corpus callosum. It may be an isolated abnormality or associated with other central nervous system abnormalities or syndromes. Clinical manifestations vary. In cases of isolated corpus callosum agenesis, symptoms may be absent or minimal. In cases that are associated with other central nervous system abnormalities or syndromes, symptoms include developmental delays, motor coordination difficulties, and vision impairment."
      },
      "child_count": 4,
      "reference_id": "MONDO:0009022"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 3690,
      "label": "coloboma"
    },
    {
      "id": 4016,
      "label": "amenorrhea"
    },
    {
      "id": 10275,
      "label": "corpus callosum, agenesis of"
    }
  ]
}