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bn:02065169n
Noun Concept
Categories: Cell surface receptor deficiencies, Visual disturbances and blindness, Articles with short description, Rare diseases
EN
Leber congenital amaurosis  Leber's amaurosis  Amaurosis congenita of Leber  Amaurosis congenita of Leber, type 1  Amaurosis congenita of Leber, type 2
EN
Leber congenital amaurosis is a rare inherited eye disease that appears at birth or in the first few months of life. Wikipedia
Definitions
Relations
Sources
EN
Leber congenital amaurosis is a rare inherited eye disease that appears at birth or in the first few months of life. Wikipedia
Retinal disease that is characterized by nystagmus, sluggish or no pupillary responses, and severe vision loss or blindness Wikidata
IS A
rare disease
retinopathy
GENETIC ASSOCIATION
GUCY2D
HEALTH SPECIALTY
ophthalmology
NAMED AFTER
Theodor Leber
Wikipedia
EN
Leber congenital amaurosis
Wikidata
EN
Leber congenital amaurosis
Wikipedia Redirections
EN
Amaurosis congenita of Leber, Amaurosis congenita of Leber, type 1, Amaurosis congenita of Leber, type 2, congenital amaurosis, Leber's amaurosis, Leber's congenital amaurosis, Leber amaurosis
Wikidata Alias
EN
AMAUROSIS CONGENITA OF LEBER I, LCA, Leber's amaurosis, Leber's congenital amaurosis, Leber's disease, Leber congenital amaurosis type 13, Leber congenital amaurosis type 14

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