Search Ontology:
Human Disease

Leber congenital amaurosis 9

Term ID
DOID:0110005
Synonyms
  • LCA9
Definition
A Leber congenital amaurosis that has_material_basis_in mutation in the NMNAT1 gene on chromosome 1p36. https://www.ncbi.nlm.nih.gov/pubmed/22842230
References
Ontology
Human Disease   ( DOID:0110005 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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