Concept information
...
Genetic disease
Hereditary disease
Autosomal hereditary disorder
Dominant hereditary disorder, NOS
...
Disorder of eye proper (disorder)
Anomaly of eye (disorder)
Congenital anomaly of eye
Microphthalmos
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Disorder of eye proper (disorder)
Anomaly of eye (disorder)
Congenital anomaly of eye
Microphthalmos
...
Disorder of eye proper (disorder)
Anomaly of eye (disorder)
Congenital anomaly of eye
Microphthalmos
...
Disorder of eye proper (disorder)
Anomaly of eye (disorder)
Congenital anomaly of eye
Microphthalmos
...
Disorder of eye proper (disorder)
Anomaly of eye (disorder)
Congenital anomaly of eye
Microphthalmos
...
Disorder of eye proper (disorder)
Anomaly of eye (disorder)
Congenital anomaly of eye
Microphthalmos
Preferred term
Syndromic microphthalmia due to orthodenticle homeobox 2 mutation (disorder)
Type
-
http://www.irandoc.ac.ir/onto/irandoc-meta/Concept
Broader concept
Associated morphology
Finding site
Is a
- 363070008
- 363343008
- Dominant hereditary disorder, NOS
- Microphthalmos
Occurrence
Pathological process
In other languages
URI
http://www.irandoc.acir/onto/irandoc/718761007
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