{
  "id": 10863,
  "label": "Morquio syndrome C",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0009647",
  "properties": {
    "xrefs": [
      "GARD:0007059",
      "MEDGEN:443986",
      "MESH:C536247",
      "OMIM:252300",
      "UMLS:C2931140"
    ],
    "synonyms": [
      "Morquio syndrome C",
      "Morquio syndrome type C",
      "Morquio syndrome, Nonkeratosulfate-Excreting type"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 18860,
      "label": "mucopolysaccharidosis type 4",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4370,
        19111
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:12804",
          "GARD:0012562",
          "MEDGEN:44513",
          "MedDRA:10028095",
          "NANDO:1200105",
          "NANDO:2200550",
          "NCIT:C61263",
          "NORD:1455",
          "Orphanet:582",
          "SCTID:378007",
          "UMLS:C0026707",
          "icd11.foundation:2078241550"
        ],
        "synonyms": [
          "MPS4",
          "MPSIV",
          "Morquio disease",
          "Morquio syndrome",
          "Mucopolysaccharidosis IV",
          "eccentro-osteochondrodysplasia",
          "eccentrochondrodysplasia",
          "eccentroosteochondrodysplasia",
          "mucopolysaccharidosis IV",
          "mucopolysaccharidosis type 4",
          "mucopolysaccharidosis type IV",
          "MPS IV - Morquio syndrome A",
          "MPS IV - Morquio syndrome B",
          "Morquio A disease",
          "Morquio syndrome A",
          "deficiency of N-acetylgalactosamine-6-sulphatase",
          "galactosamine-6-sulfatase deficiency",
          "mucopolysaccharidosis type IVA",
          "mucopolysaccharidosis type IVB",
          "mucopolysaccharidosis, MPS-IV-A"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "A lysosomal storage disease belonging to the group of mucopolysaccharidoses, and characterized by spondylo-epiphyso-metaphyseal dysplasia. It exists in two forms, A and B."
      },
      "child_count": 6,
      "reference_id": "MONDO:0018938"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 18860,
      "label": "mucopolysaccharidosis type 4"
    }
  ]
}