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Disease Night Blindness, Congenital Stationary, Autosomal Dominant 2

Name Night Blindness, Congenital Stationary, Autosomal Dominant 2
Synonyms CSNBAD2 | Night Blindness, Congenital Stationary, Rambusch Type
Categories Eye disease | Genetic disease (inborn)
MeSH® ID C566869
OMIM® ID 163500

Top ↑ Ancestors

1. DiseasesEye Diseases Has associated chemicals Has associated genes Has associated exposure references Eye Diseases, Hereditary Has associated chemicals Has associated genes Night Blindness, Congenital Stationary, Autosomal Dominant 2 Has associated chemicals Has associated genes
2. DiseasesEye Diseases Has associated chemicals Has associated genes Has associated exposure references Vision Disorders Has associated chemicals Has associated genes Night Blindness Has associated chemicals Has associated genes Night Blindness, Congenital Stationary, Autosomal Dominant 2 Has associated chemicals Has associated genes
3. DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities Has associated chemicals Has associated genes Has associated exposure references Genetic Diseases, Inborn Has associated chemicals Has associated genes Has associated exposure references Eye Diseases, Hereditary Has associated chemicals Has associated genes Night Blindness, Congenital Stationary, Autosomal Dominant 2 Has associated chemicals Has associated genes

Top ↑ Descendants

None.