Search Ontology:
Human Disease

Leber congenital amaurosis 19

Term ID
DOID:0081169
Synonyms
Definition
A Leber congenital amaurosis that has_material_basis_in mutation in the USP45 gene on chromosome 6q16. https://pubmed.ncbi.nlm.nih.gov/3057356/
References
Ontology
Human Disease   ( DOID:0081169 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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