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Renal Cell Neoplasia Tables: Recurrent Cytogenomic Alterations
(view source)
Revision as of 00:01, 15 January 2021
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00:01, 15 January 2021
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|Germline susceptibility
|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)
| colspan="2" |''[[FCLN]]'' (Birt-Hogg-Dube syndrome)
Kilannin.Krysiak
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