Concept information
...
Genetic disease
Hereditary disease
Autosomal hereditary disorder
Dominant hereditary disorder, NOS
...
Disorder of eye proper (disorder)
Anomaly of eye (disorder)
Degenerative disorder of globe
Degeneration of retina
...
Disorder of eye proper (disorder)
Anomaly of eye (disorder)
Degenerative disorder of globe
Degeneration of retina
...
Disorder of eye proper (disorder)
Anomaly of eye (disorder)
Degenerative disorder of globe
Degeneration of retina
...
Disorder of eye proper (disorder)
Anomaly of eye (disorder)
Degenerative disorder of globe
Degeneration of retina
...
Disorder of eye proper (disorder)
Anomaly of eye (disorder)
Degenerative disorder of globe
Degeneration of retina
Preferred term
LAMA5-related multisystemic syndrome
Type
-
http://www.irandoc.ac.ir/onto/irandoc-meta/Concept
Broader concept
Associated morphology
Finding site
Is a
- 106018006
- 238980001
- 239091003
- 363058009
- 363185004
- 363343008
- 54767005
- Degeneration of retina
- Dominant hereditary disorder, NOS
Occurrence
In other languages
-
Persian
URI
http://www.irandoc.acir/onto/irandoc/1217370006
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