xeroderma pigmentosum group G
(Q32143789)
xeroderma pigmentosum that has material basis in homozygous or compound heterozygous mutation in the ERCC5 gene on chromosome 13q33
xeroderma pigmentosum that has material basis in homozygous or compound heterozygous mutation in the ERCC5 gene on chromosome 13q33
Language:
Current Data About
xeroderma pigmentosum group G
| (P31) |
(Q112193867)
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| (P279) |
(Q612693)
(Q29014951)
(Q55345957)
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| (P1748) |
C3969
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| (P1995) |
(Q1071953)
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| (P2293) |
(Q17917470)
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| (P2888) |
http://purl.obolibrary.org/obo/DOID_0110849
http://identifiers.org/doid/DOID:0110849
http://www.orpha.net/ORDO/Orphanet_1466 http://www.orpha.net/ORDO/Orphanet_191 http://www.orpha.net/ORDO/Orphanet_220295 http://www.orpha.net/ORDO/Orphanet_276267 http://www.orpha.net/ORDO/Orphanet_910 |
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| (P5008) |
(Q4099686)
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other details
| aliases |
XP7 xeroderma pigmentosum VII XPG XP group G XP-G xeroderma pigmentosum, complementation group G Xeroderma Pigmentosum, Complementation Group type G Xp, Group G Xeroderma Pigmentosum 7 Xeroderma Pigmentosum, Type G/Cockayne Syndrome XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP G; XPG xeroderma pigmentosum group type G |
| description | xeroderma pigmentosum that has material basis in homozygous or compound heterozygous mutation in the ERCC5 gene on chromosome 13q33 |
External Links
| (P492) |
278780
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| (P699) |
DOID:0110849
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| (P1550) |
276267
|
| (P2892) |
C0268141
C1851443 C1968561 |
| (P4229) |
Q82.1
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| (P4317) |
5629
|
| (P5270) |
MONDO_0010216
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| (P11430) |
DI-01161
|