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 )
- is a type of
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