congenital stationary night blindness autosomal dominant 1
(Q32143975)
A congenital stationary night blindness characterized by autosomal dominant inheritance that has material basis in mutations in the RHO gene on chromosome 3q22.1.
A congenital stationary night blindness characterized by autosomal dominant inheritance that has material basis in mutations in the RHO gene on chromosome 3q22.1.
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Current Data About
congenital stationary night blindness autosomal dominant 1
| (P31) |
(Q929833)
(Q112193867) |
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| (P279) |
(Q18553290)
(Q200779)
(Q18553439)
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| (P2293) |
(Q14859555)
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| (P2888) |
http://purl.obolibrary.org/obo/DOID_0110862
http://identifiers.org/doid/DOID:0110862
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| (P5008) |
(Q4099686)
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other details
| aliases |
rhodopsin-related congenital stationary night blindness CSNBAD1 NIGHT BLINDNESS, CONGENITAL STATIONARY, AUTOSOMAL DOMINANT 1; CSNBAD1 congenital stationary night blindness autosomal dominant type 1 Night Blindness, Congenital Stationary, Autosomal Dominant type 1 Night Blindness, Congenital Stationary, Rhodopsin-Related NIGHT BLINDNESS, CONGENITAL STATIONARY, AUTOSOMAL DOMINANT 1 |
| description | A congenital stationary night blindness characterized by autosomal dominant inheritance that has material basis in mutations in the RHO gene on chromosome 3q22.1. |
External Links
| (P486) |
C566474
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| (P492) |
610445
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| (P699) |
DOID:0110862
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| (P2892) |
C1864869
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| (P5270) |
MONDO_0012498
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| (P11430) |
DI-00371
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