Search Ontology:
Human Disease
Leber congenital amaurosis 9
- Term ID
- DOID:0110005
- Synonyms
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- 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
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- ICD10CM:H35.5
- MIM:608553
- Ontology
- Human Disease ( DOID:0110005 )
- is a type of
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Zebrafish Models