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Disease Sveinsson Chorioretinal Atrophy

Name Sveinsson Chorioretinal Atrophy
Synonyms AA | Atrophia Areata | Helicoidal Peripapillary Chorioretinal Degeneration | HPCD | Peripapillary Chorioretinal Degeneration, Icelandic Type | SCRA
Categories Eye disease | Genetic disease (inborn)
MeSH® ID C566236
OMIM® ID 108985

Top ↑ Ancestors

1. DiseasesEye Diseases Has associated chemicals Has associated genes Has associated phenotype references Has associated exposure references Corneal Diseases Has associated chemicals Has associated genes Has associated phenotype references Has associated exposure references Corneal Dystrophies, Hereditary Has associated chemicals Has associated genes Has associated phenotype references Sveinsson Chorioretinal Atrophy Has associated chemicals Has associated genes Has associated phenotype references
2. DiseasesEye Diseases Has associated chemicals Has associated genes Has associated phenotype references Has associated exposure references Eye Diseases, Hereditary Has associated chemicals Has associated genes Has associated phenotype references Corneal Dystrophies, Hereditary Has associated chemicals Has associated genes Has associated phenotype references Sveinsson Chorioretinal Atrophy Has associated chemicals Has associated genes Has associated phenotype references
3. DiseasesEye Diseases Has associated chemicals Has associated genes Has associated phenotype references Has associated exposure references Retinal Diseases Has associated chemicals Has associated genes Has associated phenotype references Has associated exposure references Retinal Degeneration Has associated chemicals Has associated genes Has associated phenotype references Has associated exposure references Sveinsson Chorioretinal Atrophy Has associated chemicals Has associated genes Has associated phenotype references
4. DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities Has associated chemicals Has associated genes Has associated phenotype references Has associated exposure references Genetic Diseases, Inborn Has associated chemicals Has associated genes Has associated phenotype references Has associated exposure references Eye Diseases, Hereditary Has associated chemicals Has associated genes Has associated phenotype references Corneal Dystrophies, Hereditary Has associated chemicals Has associated genes Has associated phenotype references Sveinsson Chorioretinal Atrophy Has associated chemicals Has associated genes Has associated phenotype references

Top ↑ Descendants

None.