{
  "id": 13908,
  "label": "thrombophilia due to protein S deficiency, autosomal dominant",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0012868",
  "properties": {
    "xrefs": [
      "DOID:0111900",
      "GARD:0018568",
      "MEDGEN:479841",
      "MESH:C567077",
      "MedDRA:10068370",
      "OMIM:612336",
      "Orphanet:26349",
      "UMLS:C3278211"
    ],
    "synonyms": [
      "autosomal dominant hereditary thrombophilia due to congenital protein S deficiency",
      "hereditary thrombophilia due to congenital protein S deficiency, autosomal dominant",
      "thrombophilia 5 due to protein S deficiency, autosomal dominant",
      "thrombophilia due to protein S deficiency, autosomal dominant",
      "THPH5",
      "protein S acquired deficiency"
    ],
    "categories": [
      {
        "ref": "MONDO:0005570",
        "name": "hematologic disorder"
      }
    ],
    "definition": "Autosomal dominant form of hereditary thrombophilia due to congenital protein S deficiency."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 2903,
      "label": "autosomal dominant disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2905
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050736",
          "ICD9:758.5",
          "MEDGEN:539206",
          "SCTID:11164009",
          "UMLS:C0265385"
        ],
        "synonyms": [
          "autosomal dominant disease or disorder",
          "autosomal dominant hereditary disorder",
          "autosomal dominant inherited disorder",
          "disease or disorder, autosomal dominant",
          "disease, autosomal dominant"
        ],
        "definition": "Autosomal dominant form of disease."
      },
      "child_count": 192,
      "reference_id": "MONDO:0000426"
    },
    {
      "id": 19022,
      "label": "hereditary thrombophilia due to congenital protein S deficiency",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4412,
        23980
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0111905",
          "GARD:0016543",
          "MEDGEN:748876",
          "Orphanet:743",
          "UMLS:C2584611",
          "icd11.foundation:1305244529"
        ],
        "synonyms": [
          "autosomal recessive thrombophilia due to congenital protein S deficiency",
          "hereditary thrombophilia due to congenital protein S deficiency",
          "severe hereditary thrombophilia due to congenital protein S deficiency"
        ],
        "categories": [
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "Congenital protein S deficiency is an inherited coagulation disorder characterized by recurrent venous thrombosis symptoms due to reduced synthesis and/or activity levels of protein S."
      },
      "child_count": 4,
      "reference_id": "MONDO:0019144"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 2903,
      "label": "autosomal dominant disease"
    },
    {
      "id": 19022,
      "label": "hereditary thrombophilia due to congenital protein S deficiency"
    }
  ]
}