Concept information
Preferred term
بیماری نوری آتیپیک ناشی از مونوزومی Xp11.3 (اختلال)
Type
-
http://www.irandoc.ac.ir/onto/irandoc-meta/Concept
Broader concept
Associated morphology
Finding site
- 278145009
- شبکیه
- کروموزوم جنسی X
Is a
Occurrence
Pathological process
In other languages
URI
http://www.irandoc.acir/onto/irandoc/733626002
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