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algorithms.tnm.1.6.tables.ssf5_npf.json Maven / Gradle / Ivy

{
  "id" : "ssf5_npf",
  "algorithm" : "tnm",
  "version" : "1.6",
  "name" : "SSF5",
  "title" : "Site-Specific Factor 5",
  "subtitle" : "Chromosome 3 Status",
  "notes" : "**Note:**  The loss of chromosome 3 (also termed loss of heterozygosity (LOH) in chromosome 3) is a common genetic abnormality in ocular melanoma. Monosomy 3 (i.e., only one copy of chromosome 3) has consistently been associated with death from metastasis in choroidal and ciliary body melanoma.",
  "last_modified" : "2018-02-02T14:54:19.364Z",
  "definition" : [ {
    "key" : "ssf5",
    "name" : "Code",
    "type" : "INPUT"
  }, {
    "key" : "description",
    "name" : "Description",
    "type" : "DESCRIPTION"
  } ],
  "rows" : [ [ "000", "No loss of chromosome 3" ], [ "010", "Partial loss of chromosome 3" ], [ "020", "Complete loss of chromosome 3" ], [ "030", "Loss of chromosome 3, NOS" ], [ "988", "Not applicable: Information not collected for this case" ], [ "997", "Test ordered, results not available" ], [ "998", "Test not done (test not ordered  and not performed)" ], [ "999", "Unknown or no information\nNot documented in patient record" ] ]
}