{
  "id": 21723,
  "label": "megacystis-microcolon-intestinal hypoperistalsis syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0025986",
  "properties": {
    "xrefs": [
      "GARD:0027919",
      "MEDGEN:296125",
      "OMIMPS:249210",
      "UMLS:C1608393"
    ],
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      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0004335",
        "name": "digestive system disorder"
      }
    ]
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 5,
  "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": 5714,
      "label": "hereditary disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29382
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:630",
          "EFO:0000508",
          "ICD9:799.89",
          "MEDGEN:5527",
          "MESH:D030342",
          "NCIT:C3101",
          "SCTID:32895009",
          "UMLS:C0019247"
        ],
        "synonyms": [
          "genetic condition",
          "genetic disease",
          "genetic disorder",
          "hereditary disease",
          "hereditary disease or disorder",
          "hereditary diseases",
          "inherited disease",
          "inherited genetic disease",
          "molecular disease",
          "Mendelian disease",
          "familial disorder",
          "inborn disorder"
        ],
        "definition": "A disease that is caused by genetic modifications where those modifications are inherited from a parent's genome."
      },
      "child_count": 1925,
      "reference_id": "MONDO:0003847"
    },
    {
      "id": 20415,
      "label": "intestinal motility disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6756
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:586448",
          "UMLS:C0400865"
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        "synonyms": [
          "disorder of intestinal motility"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          }
        ],
        "definition": "A disease that has its basis in the disruption of intestinal motility."
      },
      "child_count": 15,
      "reference_id": "MONDO:0021189"
    }
  ],
  "children": [
    {
      "id": 21719,
      "label": "megacystis-microcolon-intestinal hypoperistalsis syndrome 2",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        21723
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0016447",
          "MEDGEN:1788773",
          "OMIM:619351",
          "UMLS:C5543476"
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        "synonyms": [
          "MMIHS2"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0025708"
    },
    {
      "id": 21868,
      "label": "megacystis-microcolon-intestinal hypoperistalsis syndrome 3",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        21723
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0027924",
          "MEDGEN:1780019",
          "OMIM:619362",
          "UMLS:C5543513"
        ],
        "synonyms": [
          "MMIHS3",
          "megacystis-microcolon-intestinal hypoperistalsis syndrome 3"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0030294"
    },
    {
      "id": 21869,
      "label": "megacystis-microcolon-intestinal hypoperistalsis syndrome 4",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        21723
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0027925",
          "MEDGEN:1783600",
          "OMIM:619365",
          "UMLS:C5543519"
        ],
        "synonyms": [
          "MMIHS4",
          "megacystis-microcolon-intestinal hypoperistalsis syndrome 4"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0030296"
    },
    {
      "id": 21885,
      "label": "megacystis-microcolon-intestinal hypoperistalsis syndrome 5",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        21723
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0027926",
          "MEDGEN:1782906",
          "OMIM:619431",
          "UMLS:C5543636"
        ],
        "synonyms": [
          "MMIHS5",
          "megacystis-microcolon-intestinal hypoperistalsis syndrome 5"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0030329"
    },
    {
      "id": 24082,
      "label": "megacystis-microcolon-intestinal hypoperistalsis syndrome 1",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        21723
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060610",
          "GARD:0015195",
          "MEDGEN:1778116",
          "MESH:C536138",
          "NCIT:C98982",
          "OMIM:249210",
          "Orphanet:2241",
          "SCTID:253781004",
          "UMLS:C5542316"
        ],
        "synonyms": [
          "MMIH syndrome",
          "MMIHS",
          "megacystis microcolon intestinal hypoperistalsis syndrome",
          "megacystis, microcolon, hypoperistalsis syndrome",
          "megacystis, microcolon, intestinal hypoperistalsis syndrome",
          "megacystis-microcolon-intestinal hypoperistalsis syndrome",
          "megacystis-microcolon-intestinal hypoperistalsis syndrome, MMIH",
          "megacystis-microcolon-intestinal hypoperistalsis-hydronephrosis syndrome",
          "Berdon syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0100354"
    }
  ],
  "roots": [
    {
      "id": 4370,
      "label": "syndromic disease"
    },
    {
      "id": 5714,
      "label": "hereditary disease"
    },
    {
      "id": 20415,
      "label": "intestinal motility disease"
    }
  ]
}