Search Ontology:
Human Disease
Leber congenital amaurosis
- Term ID
- DOID:14791
- Synonyms
-
- LCA
- Leber's amaurosis
- Leber's congenital amaurosis
- Leber's disease
- Definition
- A retinal disease that is characterized by nystagmus, sluggish or no pupillary responses, and severe vision loss or blindness. http://en.wikipedia.org/wiki/Leber%27s_congenital_amaurosis
- References
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- GARD:634
- MESH:D057130
- MIM:PS204000
- NCI:C129075
- ORDO:65
- SNOMEDCT_US_2023_03_01:193413001
- UMLS_CUI:C0339527
- Ontology
- Human Disease ( DOID:14791 )
- is a type of
-
- has subtype
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Genes Involved
Zebrafish Models
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