Search Ontology:
Human Disease

Leber congenital amaurosis 3

Term ID
DOID:0110331
Synonyms
  • LCA3
Definition
A Leber congenital amaurosis that has_material_basis_in mutation in the SPATA7 gene on chromosome 14q31. https://www.ncbi.nlm.nih.gov/pubmed/19268277
References
Ontology
Human Disease   ( DOID:0110331 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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