Search Ontology:
Human Disease

Leber congenital amaurosis 7

Term ID
DOID:0110333
Synonyms
  • LCA7
Definition
A Leber congenital amaurosis that has_material_basis_in mutation in the CRX gene on chromosome 19q13. https://www.ncbi.nlm.nih.gov/pubmed/9537410
References
Ontology
Human Disease   ( DOID:0110333 )
Relationships
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
Your Input Welcome
We welcome your input and comments. Please use this form to recommend updates to the information in ZFIN. We appreciate as much detail as possible and references as appropriate. We will review your comments promptly.
Please check the highlighted fields and try again.
Thank you for submitting comments. Your input has been emailed to ZFIN curators who may contact you if additional information is required.
Oops. Something went wrong. Please try again later.