Usher syndrome type 1C
(Q32143522)
Usher syndrome type 1 that has material basis in homozygous or compound heterozygous mutation in the USH1C gene on chromosome 11p15
Usher syndrome type 1 that has material basis in homozygous or compound heterozygous mutation in the USH1C gene on chromosome 11p15
Language:
Current Data About
Usher syndrome type 1C
(P31) |
(Q929833)
(Q112193867) |
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(P279) |
(Q32143464)
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(P2293) |
(Q18035012)
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(P2888) |
http://purl.obolibrary.org/obo/DOID_0110830
http://identifiers.org/doid/DOID:0110830
http://www.orpha.net/ORDO/Orphanet_231169 http://www.orpha.net/ORDO/Orphanet_886 |
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(P5008) |
(Q4099686)
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other details
aliases |
Usher syndrome type I Acadian variety USH1C Usher syndrome type IC Usher Syndrome, Type I, Acadian Variety USHER SYNDROME, TYPE IC Usher syndrome, Acadian variety Usher syndrome, type 1C USHER SYNDROME, TYPE IC; USH1C |
description | Usher syndrome type 1 that has material basis in homozygous or compound heterozygous mutation in the USH1C gene on chromosome 11p15 |
External Links
(P492) |
276904
276904 |
(P699) |
DOID:0110830
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(P2892) |
C1848604
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(P4229) |
H35.5
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(P4317) |
5437
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(P5270) |
MONDO_0010171
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(P11430) |
DI-01113
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