hyperornithinemia
From Aaushi
Jump to navigation
Jump to search
[
1
]
Contents
1
Pathology
2
Genetics
3
Clinical manifestations
4
More general terms
5
References
6
Database
Pathology
gyrate
atrophy
of
choroid
&
retina
Genetics
autosomal recessive
for associated with defects in
ornithine aminotransferase
Clinical manifestations
blindness
More general terms
genetic disease
metabolic disease
References
↑
OMIM
https://mirror.omim.org/entry/258870
Database
OMIM:
https://mirror.omim.org/entry/258870
↑ Back to top
Navigation menu
Personal tools
Log in
Namespaces
Page
Discussion
English
Views
Read
View source
View history
More
Search
Navigation
Main page
Illustrative examples
Differential diagnosis
Drug interactions
Donate
Donate
Tools
What links here
Related changes
Special pages
Printable version
Permanent link
Page information
Cite this page