About: BRCA2 Syndrome     Goto   Sponge   NotDistinct   Permalink

An Entity of Type : owl:Class, within Data Space : linked.opendata.cz associated with source document(s)

AttributesValues
rdf:type
rdfs:label
  • BRCA2 Syndrome
equivalentClass
Semantic_Type
  • Disease or Syndrome
Preferred_Name
  • BRCA2 Syndrome
UMLS_CUI
  • C1332443
Legacy_Concept_Name
  • BRCA_2_Syndrome
FULL_SYN
  • BRCA2 SyndromePTNCI
  • Site Specific Early Onset Breast Cancer SyndromeSYNCI
DEFINITION
  • An autosomal dominant inherited syndrome caused by mutations in the BRCA2 gene. Patients are at high risk of developing female and male breast cancer, ovarian cancer, and other cancers including prostatic cancer, pancreatic cancer, gastric cancer, and melanoma.NCI
code
  • C36101
is someValuesFrom of
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