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Disease Retinitis Pigmentosa 32

Name Retinitis Pigmentosa 32
Synonym RP32
Categories Eye disease | Genetic disease (inborn)
MeSH® ID C563689
OMIM® ID 609913

Top ↑ Ancestors

1. DiseasesEye Diseases Has associated chemicals Has associated genes Has associated exposure references Eye Diseases, Hereditary Has associated chemicals Has associated genes Retinitis Pigmentosa Has associated chemicals Has associated genes Retinitis Pigmentosa 32 Has associated genes
2. DiseasesEye Diseases Has associated chemicals Has associated genes Has associated exposure references Retinal Diseases Has associated chemicals Has associated genes Has associated exposure references Retinal Degeneration Has associated chemicals Has associated genes Has associated exposure references Retinal Dystrophies Has associated chemicals Has associated genes Retinitis Pigmentosa Has associated chemicals Has associated genes Retinitis Pigmentosa 32 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 Retinitis Pigmentosa Has associated chemicals Has associated genes Retinitis Pigmentosa 32 Has associated genes

Top ↑ Descendants

None.