Leber congenital amaurosis
(Q1811132)
retinal disease that is characterized by nystagmus, sluggish or no pupillary responses, and severe vision loss or blindness
retinal disease that is characterized by nystagmus, sluggish or no pupillary responses, and severe vision loss or blindness
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Current Data About
Leber congenital amaurosis
| (P31) |
(Q929833)
(Q112193867) |
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| (P138) |
(Q69692)
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| (P279) |
(Q550455)
(Q12136) |
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| (P373) |
Leber's congenital amaurosis
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| (P1748) |
C129075
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| (P1995) |
(Q161437)
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| (P2293) |
(Q18026719)
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| (P2888) |
http://purl.obolibrary.org/obo/DOID_14791
http://identifiers.org/doid/DOID:14791
http://www.orpha.net/ORDO/Orphanet_65 |
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| (P5008) |
(Q4099686)
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other details
| aliases |
AMAUROSIS CONGENITA OF LEBER I LCA Leber congenital amaurosis type 13 Leber congenital amaurosis type 14 Leber's amaurosis (disorder) Leber's congenital amaurosis Leber's disease Leber's amaurosis |
| description | retinal disease that is characterized by nystagmus, sluggish or no pupillary responses, and severe vision loss or blindness |
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