{
  "id": 17852,
  "label": "Proteus-like syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0017571",
  "properties": {
    "xrefs": [
      "GARD:0012801",
      "MEDGEN:356222",
      "NCIT:C179930",
      "Orphanet:2969",
      "SCTID:716862002",
      "UMLS:C1866398"
    ],
    "synonyms": [
      "Cohen-Hayden syndrome",
      "Proteus like syndrome intellectual disability eye defect",
      "Proteus like syndrome mental retardation eye defect"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      },
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      }
    ],
    "definition": "Proteus-like syndrome describes patients who do not meet the diagnostic criteria for Proteus syndrome but who share a multitude of characteristic clinical features of the disease."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 4198,
      "label": "integumentary system disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29379
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:16",
          "EFO:0010285",
          "MEDGEN:712400",
          "SCTID:128598002",
          "UMLS:C1290011"
        ],
        "synonyms": [
          "disease of integumental system",
          "disease or disorder of integumental system",
          "disorder of integumental system",
          "integumental system disease",
          "integumental system disease or disorder",
          "integumentary disease",
          "disorder of integument"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "A disease involving the integumental system."
      },
      "child_count": 36,
      "reference_id": "MONDO:0002051"
    },
    {
      "id": 17900,
      "label": "PTEN hamartoma tumor syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2903,
        16218,
        19507
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080191",
          "GARD:0012800",
          "MEDGEN:368366",
          "NCIT:C179915",
          "NORD:1631",
          "Orphanet:306498",
          "SCTID:722859001",
          "UMLS:C1959582"
        ],
        "synonyms": [
          "PHTS",
          "PTEN hamartoma tumor syndrome",
          "PTEN-related Hamartoma tumor syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "An autosomal dominant syndrome caused by pathogenic variants in the PTEN gene, characterized by hamartomas, overgrowth, neurodevelopmental disorders and an increased risk of various cancers, including breast, thyroid, and endometrial cancer. PHTS encompasses Cowden syndrome, Bannayan-Riley-Ruvalcaba syndrome, and Proteus-like syndrome."
      },
      "child_count": 12,
      "reference_id": "MONDO:0017623"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 4198,
      "label": "integumentary system disorder"
    },
    {
      "id": 17900,
      "label": "PTEN hamartoma tumor syndrome"
    }
  ]
}