Renal Cell Neoplasia Tables: Recurrent Cytogenomic Alterations: Difference between revisions

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@@ Line 314: / Line 314: @@
 |-
 |Germline susceptibility
-|§ mainly ''[[VHL]]'' (von Hippel-Lindau Syndrome)
+|
+* mainly ''[[VHL]]'' (von Hippel-Lindau Syndrome)
-§ ''[[PTEN]]'' (Cowden Syndrome)
+* ''[[PTEN]]'' (Cowden Syndrome)
+* ''[[FLCN]]'' (Birt-Hogg-Dube syndrome)
-§ ''[[FLCN]]'' (Birt-Hogg-Dube syndrome)
+* ''[[TSC1]]'' and ''[[TSC2]]'' (tuberous sclerosis)
+* ''[[SDHB]] (most common), [[SDHC]] (less common), [[SDHA]] (rare), [[SDHD]] (rare)'' (succinate dehydrogenase deficient RCC)
-§ ''[[TSC1]]'' and ''[[TSC2]]'' (tuberous sclerosis)
+|
+* ''[[MET]]'' (Hereditary papillary RCC)
-§ ''[[SDHB]] (most common), [[SDHC]] (less common), [[SDHA]] (rare), [[SDHD]] (rare)'' (succinate dehydrogenase deficient RCC)
+|
-|§ ''[[MET]]'' (Hereditary papillary RCC)
+* ''[[FH]]'' (Hereditary leiomyomatosis and RCC)
-|§ ''[[FH]]'' (Hereditary leiomyomatosis and RCC)
 |
 | colspan="2" |''[[FCLN]]'' (Birt-Hogg-Dube syndrome)