Search Ontology:
Human Disease

Leber congenital amaurosis 8

Term ID
DOID:0110079
Synonyms
  • LCA8
Definition
A Leber congenital amaurosis that is characterized by night blindness and thick unlaminated retinas and has_material_basis_in mutation in the CRB1 gene on chromosome 1q31-q32. https://www.ncbi.nlm.nih.gov/pubmed/11231775
References
Ontology
Human Disease   ( DOID:0110079 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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