{
  "id": 21932,
  "label": "Galloway-Mowat syndrome 9",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0030471",
  "properties": {
    "xrefs": [
      "GARD:0025570",
      "MEDGEN:1794226",
      "OMIM:619603",
      "UMLS:C5562016"
    ],
    "synonyms": [
      "GAMOS9"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 10847,
      "label": "Galloway-Mowat syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4370,
        7611
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080694",
          "GARD:0000065",
          "MEDGEN:167086",
          "MESH:C537548",
          "NANDO:1200713",
          "NANDO:2200120",
          "NANDO:2201385",
          "NCIT:C132195",
          "NORD:1171",
          "OMIMPS:251300",
          "Orphanet:2065",
          "SCTID:721297008",
          "UMLS:C0795949"
        ],
        "synonyms": [
          "Galloway syndrome",
          "Galloway-Mowat syndrome",
          "microcephaly, hiatal hernia and nephrotic syndrome",
          "microcephaly-hiatus hernia-nephrotic syndrome",
          "nephrosis-microcephaly syndrome",
          "nephrosis-neuronal dysmigration syndrome",
          "spinocerebellar ataxia, autosomal recessive 5",
          "GAMOS",
          "Galloway Mowat syndrome",
          "cerebellar ataxia with intellectual disability, optic atrophy, and skin abnormalities",
          "cerebellar ataxia with mental retardation, optic atrophy, and skin abnormalities",
          "hiatal hernia-microcephaly-nephrosis, Galloway type",
          "microcephaly nephrosis syndrome",
          "microcephaly, hiatal hernia, and nephrotic syndrome",
          "nephrosis neuronal dysmigration syndrome",
          "spinocerebellar ataxia, autosomal recessive 5, formerly"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "Galloway syndrome is characterized by the association of nephrotic syndrome and central nervous system anomalies."
      },
      "child_count": 20,
      "reference_id": "MONDO:0009627"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 10847,
      "label": "Galloway-Mowat syndrome"
    }
  ]
}