retinitis pigmentosa 7
(Q27677782)
retinitis pigmentosa that has material basis in mutation in the PRPH2 gene on chromosome 6p21
retinitis pigmentosa that has material basis in mutation in the PRPH2 gene on chromosome 6p21
Language:
Current Data About
retinitis pigmentosa 7
(P31) |
(Q929833)
(Q112193867) |
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(P279) |
(Q847057)
(Q200779)
(Q10267817)
(Q66299868)
(Q18553439)
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(P2293) |
(Q18031205)
(Q18031081)
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(P2888) |
http://purl.obolibrary.org/obo/DOID_0110383
http://identifiers.org/doid/DOID:0110383
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(P5008) |
(Q4099686)
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other details
aliases |
RP7 RETINITIS PIGMENTOSA 7; RP7 Leber Congenital Amaurosis 18 RETINITIS PIGMENTOSA 7 retinitis pigmentosa type 7 RP 7 Retinitis Pigmentosa 7, Digenic |
description | retinitis pigmentosa that has material basis in mutation in the PRPH2 gene on chromosome 6p21 |
External Links
(P492) |
608133
608133 |
(P699) |
DOID:0110383
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(P2892) |
C1842475
C2675553 C2675552 |
(P4229) |
H35.5
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(P4317) |
10386
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(P5270) |
MONDO_0011974
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(P11430) |
DI-00975
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