{
  "id": 10847,
  "label": "Galloway-Mowat syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0009627",
  "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."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 10,
  "parents": [
    {
      "id": 4370,
      "label": "syndromic disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29379
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:225",
          "MEDGEN:11688",
          "MESH:D013577",
          "NCIT:C28193",
          "OGMS:0000086",
          "UMLS:C0039082"
        ],
        "synonyms": [
          "cluster, symptom",
          "clusters, symptom",
          "symptom cluster",
          "symptom clusters",
          "syndrome",
          "syndrome associated with disease or disorder",
          "syndromes",
          "syndromic disease",
          "syndromic disease or disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "A group of signs, symptoms, and clinicopathological characteristics that may or may not have a genetic basis and collectively define an abnormal condition."
      },
      "child_count": 1182,
      "reference_id": "MONDO:0002254"
    },
    {
      "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"
    }
  ],
  "children": [
    {
      "id": 21932,
      "label": "Galloway-Mowat syndrome 9",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        10847
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0025570",
          "MEDGEN:1794226",
          "OMIM:619603",
          "UMLS:C5562016"
        ],
        "synonyms": [
          "GAMOS9"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0030471"
    },
    {
      "id": 21937,
      "label": "Galloway-Mowat syndrome 10",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        10847
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0025575",
          "MEDGEN:1794230",
          "OMIM:619609",
          "UMLS:C5562020"
        ],
        "synonyms": [
          "GAMOS10"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0030476"
    },
    {
      "id": 22366,
      "label": "Galloway-Mowat syndrome 6",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        10847
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0016343",
          "MEDGEN:1674560",
          "OMIM:618347",
          "UMLS:C5193043"
        ],
        "synonyms": [
          "GALLOWAY-MOWAT SYNDROME 6",
          "GAMOS6"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0032691"
    },
    {
      "id": 22367,
      "label": "Galloway-Mowat syndrome 7",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        10847
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0016344",
          "MEDGEN:1679283",
          "OMIM:618348",
          "UMLS:C5193044"
        ],
        "synonyms": [
          "GALLOWAY-MOWAT SYNDROME 7",
          "GAMOS7"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0032692"
    },
    {
      "id": 22368,
      "label": "Galloway-Mowat syndrome 8",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        10847
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0016345",
          "MEDGEN:1675829",
          "OMIM:618349",
          "UMLS:C5193045"
        ],
        "synonyms": [
          "GALLOWAY-MOWAT SYNDROME 8",
          "GAMOS8"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0032693"
    },
    {
      "id": 22596,
      "label": "Galloway-Mowat syndrome 1",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        10847
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060364",
          "GARD:0015199",
          "MEDGEN:1634188",
          "OMIM:251300",
          "UMLS:C4551772"
        ],
        "synonyms": [
          "Galloway-Mowat syndrome 1",
          "GAMOS1",
          "Galloway syndrome",
          "cerebellar ataxia with intellectual disability, optic atrophy, and skin abnormalities",
          "cerebellar ataxia with mental retardation, optic atrophy, and skin abnormalities",
          "microcephaly, hiatal hernia, and nephrotic syndrome",
          "nephrosis-microcephaly syndrome",
          "nephrosis-neuronal dysmigration syndrome",
          "spinocerebellar ataxia, autosomal recessive 5",
          "spinocerebellar ataxia, autosomal recessive 5, formerly"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0033005"
    },
    {
      "id": 22597,
      "label": "Galloway-Mowat syndrome 2, X-linked",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        10847
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080244",
          "GARD:0015281",
          "MEDGEN:1625619",
          "OMIM:301006",
          "UMLS:C4538784"
        ],
        "synonyms": [
          "Galloway-Mowat syndrome 2, X-linked",
          "Galloway-Mowat syndrome 2, X-linked, X-linked recessive",
          "GAMOS2",
          "Galloway-Mowat syndrome 2"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0033006"
    },
    {
      "id": 22598,
      "label": "Galloway-Mowat syndrome 3",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        10847
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080245",
          "GARD:0016247",
          "MEDGEN:1627611",
          "OMIM:617729",
          "UMLS:C4540266"
        ],
        "synonyms": [
          "Galloway-Mowat syndrome 3",
          "GAMOS3"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0033007"
    },
    {
      "id": 22599,
      "label": "Galloway-Mowat syndrome 4",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        10847
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080246",
          "GARD:0016248",
          "MEDGEN:1613511",
          "OMIM:617730",
          "UMLS:C4540270"
        ],
        "synonyms": [
          "Galloway-Mowat syndrome 4",
          "GAMOS4"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0033008"
    },
    {
      "id": 22600,
      "label": "Galloway-Mowat syndrome 5",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        10847
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080247",
          "GARD:0016249",
          "MEDGEN:1617227",
          "OMIM:617731",
          "UMLS:C4540274"
        ],
        "synonyms": [
          "Galloway-Mowat syndrome 5",
          "GAMOS5"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0033009"
    }
  ],
  "roots": [
    {
      "id": 4370,
      "label": "syndromic disease"
    },
    {
      "id": 7611,
      "label": "autosomal recessive disease"
    }
  ]
}