{
  "id": 6811,
  "label": "psoriasis",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0005083",
  "properties": {
    "xrefs": [
      "DOID:8893",
      "EFO:0000676",
      "ICD10CM:L40",
      "ICD10WHO:L40",
      "ICD9:696",
      "ICD9:696.1",
      "ICD9:696.5",
      "ICD9:696.8",
      "MEDGEN:10997",
      "MESH:D011565",
      "NCIT:C3346",
      "OMIMPS:177900",
      "SCTID:9014002",
      "UMLS:C0033860",
      "icd11.foundation:63698555"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      },
      {
        "ref": "MONDO:0005046",
        "name": "immune system disorder"
      }
    ],
    "definition": "An autoimmune condition characterized by red, well-delineated plaques with silvery scales that are usually on the extensor surfaces and scalp. They can occasionally present with these manifestations: pustules; erythema and scaling in intertriginous areas, and erythroderma, that are often distributed on extensor surfaces and scalp."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 3,
  "parents": [
    {
      "id": 4496,
      "label": "dermatitis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6820,
        20399
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:2723",
          "ICD9:692.9",
          "MEDGEN:849741",
          "MESH:D003872",
          "NCIT:C2983",
          "SCTID:43116000",
          "UMLS:C3875321"
        ],
        "synonyms": [
          "inflammation of skin",
          "inflammation of the skin",
          "inflammation of zone of skin",
          "inflammatory skin disease",
          "skin inflammation",
          "zone of skin inflammation"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "An inflammatory process affecting the skin. Signs include red rash, itching, and blister formation. Representative examples are contact dermatitis, atopic dermatitis, and seborrheic dermatitis."
      },
      "child_count": 66,
      "reference_id": "MONDO:0002406"
    },
    {
      "id": 6778,
      "label": "immune system disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29379
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:2914",
          "EFO:0000540",
          "ICD9:279",
          "ICD9:279.1",
          "ICD9:279.10",
          "ICD9:279.19",
          "ICD9:279.4",
          "ICD9:279.49",
          "ICD9:279.8",
          "ICD9:279.9",
          "MEDGEN:5759",
          "MESH:D007154",
          "NANDO:1100004",
          "NANDO:2100202",
          "NCIT:C3507",
          "SCTID:414029004",
          "UMLS:C0021053"
        ],
        "synonyms": [
          "disease of immune system",
          "disease or disorder of immune system",
          "disorder of immune system",
          "immune disease",
          "immune disorder",
          "immune dysfunction",
          "immune system disease or disorder",
          "immune system disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "A disorder resulting from an abnormality in the immune system."
      },
      "child_count": 47,
      "reference_id": "MONDO:0005046"
    },
    {
      "id": 23867,
      "label": "hereditary skin disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        6820
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MESH:D012873",
          "SCTID:239001006"
        ],
        "synonyms": [
          "disease, genetic skin",
          "diseases, genetic skin",
          "genetic skin disease",
          "genetic skin diseases",
          "genodermatosis",
          "skin disease, genetic"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "An instance of skin disease that is caused by a modification of the individual's genome."
      },
      "child_count": 228,
      "reference_id": "MONDO:0100118"
    }
  ],
  "children": [
    {
      "id": 12389,
      "label": "psoriasis 2",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6811
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080475",
          "MEDGEN:351141",
          "NANDO:2200443",
          "OMIM:602723",
          "UMLS:C1864497"
        ],
        "synonyms": [
          "CARD14 psoriasis",
          "psoriasis 2",
          "psoriasis caused by mutation in CARD14",
          "psoriasis type 2",
          "PSORS2"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "Any psoriasis in which the cause of the disease is a mutation in the CARD14 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0011269"
    },
    {
      "id": 20830,
      "label": "pustular psoriasis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6811
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "ICD9:696.1",
          "MEDGEN:508876",
          "NANDO:1200240",
          "NANDO:2100285",
          "NANDO:2201001",
          "SCTID:200973000",
          "UMLS:C0152081",
          "icd11.foundation:64081271"
        ],
        "synonyms": [
          "pustular psoriasis",
          "Pustular psoriasis"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ]
      },
      "child_count": 2,
      "reference_id": "MONDO:0022205"
    },
    {
      "id": 21210,
      "label": "guttate psoriasis",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6811
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "ICD10CM:L40.4",
          "ICD9:696.1",
          "MEDGEN:91004",
          "SCTID:37042000",
          "UMLS:C0343052",
          "icd11.foundation:1202062855"
        ],
        "synonyms": [
          "guttate psoriasis"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "A form of psoriasis characterized by a sudden onset of small, red, and scaly teardrop-shaped spots that appear on the arms, legs, and middle of the body, usually triggered by an infection."
      },
      "child_count": 0,
      "reference_id": "MONDO:0023297"
    }
  ],
  "roots": [
    {
      "id": 4496,
      "label": "dermatitis"
    },
    {
      "id": 6778,
      "label": "immune system disorder"
    },
    {
      "id": 23867,
      "label": "hereditary skin disorder"
    }
  ]
}