{
  "id": 8490,
  "label": "alacrima, congenital, autosomal dominant",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007075",
  "properties": {
    "xrefs": [
      "GARD:0018165",
      "MEDGEN:934803",
      "MESH:C566307",
      "OMIM:103420",
      "UMLS:C4310836"
    ],
    "synonyms": [
      "alacrima, congenital",
      "alacrimia congenita",
      "alacrimia congenita, autosomal dominant"
    ],
    "categories": [
      {
        "ref": "MONDO:0002022",
        "name": "disorder of orbital region"
      },
      {
        "ref": "MONDO:0024458",
        "name": "disorder of visual system"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 19417,
      "label": "isolated congenital alacrima",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4032
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0016799",
          "MEDGEN:896261",
          "Orphanet:91416",
          "SCTID:717262004",
          "UMLS:C4273963"
        ],
        "synonyms": [
          "nonsyndromic congenital alacrima"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "Congenital alacrima is characterized by deficient lacrimation (ranging from a complete absence of tears to hyposecretion of tears) that is present from birth."
      },
      "child_count": 2,
      "reference_id": "MONDO:0019627"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 19417,
      "label": "isolated congenital alacrima"
    }
  ]
}