Cockayne syndrome type 2
(Q55346084)
Cockayne syndrome caused by mutation(s) in the ERCC6 gene, encoding DNA excision repair protein ERCC-6
Cockayne syndrome caused by mutation(s) in the ERCC6 gene, encoding DNA excision repair protein ERCC-6
Language:
Current Data About
Cockayne syndrome type 2
(P31) |
(Q112193867)
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(P279) |
(Q914389)
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(P1748) |
C135726
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(P2293) |
(Q17917471)
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(P2888) |
http://www.orpha.net/ORDO/Orphanet_191
http://www.orpha.net/ORDO/Orphanet_90321 http://www.orpha.net/ORDO/Orphanet_90322 http://www.orpha.net/ORDO/Orphanet_90324 |
other details
aliases |
Cockayne Syndrome type B COCKAYNE SYNDROME B COCKAYNE SYNDROME B; CSB CSB Cockayne syndrome type II |
description | Cockayne syndrome caused by mutation(s) in the ERCC6 gene, encoding DNA excision repair protein ERCC-6 |
External Links
(P492) |
133540
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(P1550) |
90322
191 90324 90321 |
(P2892) |
C0751038
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(P4229) |
Q87.8
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(P5270) |
MONDO_0019570
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(P7807) |
1604701958
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(P11430) |
DI-00312
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