Concept information
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Genetic disease
Hereditary disease
Autosomal hereditary disorder
Dominant hereditary disorder, NOS
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Congenital malformation
Congenital malformation syndrome (disorder)
Multiple system malformation syndrome
Multiple malformation syndrome with facial defects as major feature
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Congenital malformation
Congenital malformation syndrome (disorder)
Multiple system malformation syndrome
Multiple malformation syndrome with facial defects as major feature
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Visual system disorder
Disorder of eye region (disorder)
Disorder of orbit proper (disorder)
Congenital anomaly of orbit
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Visual system disorder
Disorder of eye region (disorder)
Disorder of orbit proper (disorder)
Congenital anomaly of orbit
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Disease of head
Disorder of eye region (disorder)
Disorder of orbit proper (disorder)
Congenital anomaly of orbit
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Disease of head
Disorder of eye region (disorder)
Disorder of orbit proper (disorder)
Congenital anomaly of orbit
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Finding of head region
Disorder of eye region (disorder)
Disorder of orbit proper (disorder)
Congenital anomaly of orbit
Preferred term
Syndromic hypoplasia of orbital border (disorder)
Type
-
http://www.irandoc.ac.ir/onto/irandoc-meta/Concept
Broader concept
Associated morphology
Finding site
- 77886003
- Face
Is a
- 246913001
- 363070008
- 363343008
- Congenital anomaly of orbit
- Dominant hereditary disorder, NOS
- Multiple malformation syndrome with facial defects as major feature
Occurrence
Pathological process
In other languages
URI
http://www.irandoc.acir/onto/irandoc/717337001
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