{
  "id": 3763,
  "label": "Potter sequence",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0001558",
  "properties": {
    "xrefs": [
      "DOID:12594",
      "ICD10CM:Q60.6",
      "MEDGEN:472617",
      "NANDO:2200157",
      "NCIT:C40435",
      "SCTID:41962002",
      "UMLS:C0178426"
    ],
    "synonyms": [
      "Potter syndrome",
      "Potter's sequence",
      "Potter's syndrome",
      "oligohydramnios sequence"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0005039",
        "name": "reproductive system disorder"
      }
    ],
    "definition": "A rare, lethal congenital malformation characterized by bilateral renal agenesis and the absence or decreased volume of amniotic fluid (oligohydramnios). The presence of oligohydramnios gives rise to congenital anomalies that include hypoplastic lungs, lower extremities abnormalities, and characteristic facial features (low-set ears, widely separated eyes, nose flattening, and receding chin). Newborn infants usually die of respiratory failure."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "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": 7487,
      "label": "oligohydramnios",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7519
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:12215",
          "EFO:0007401",
          "HP:0001562",
          "ICD10CM:O41.0",
          "ICD9:658.0",
          "ICD9:658.00",
          "MEDGEN:86974",
          "MESH:D016104",
          "SCTID:59566000",
          "UMLS:C0079924",
          "icd11.foundation:262953341"
        ],
        "synonyms": [
          "oligohydramnios",
          "oligohydramnios (disease)"
        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          }
        ],
        "definition": "A lower than normal quantity of amniotic fluid in the amniotic sac as compared to normal values. Typically associated with an amniotic fluid index (AFI) of less than 5 cm or a single maximum vertical pocket (MVP) of less than 2 cm."
      },
      "child_count": 1,
      "reference_id": "MONDO:0005881"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 4370,
      "label": "syndromic disease"
    },
    {
      "id": 7487,
      "label": "oligohydramnios"
    }
  ]
}