Concept information
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Disorder of anterior segment of eye
Disorder of lens
Congenital anomaly of lens
Congenital cataract
...
Disorder of anterior segment of eye
Disorder of lens
Congenital anomaly of lens
Congenital cataract
...
Disorder of anterior segment of eye
Disorder of lens
Congenital anomaly of lens
Congenital cataract
...
Disorder of anterior segment of eye
Disorder of lens
Congenital anomaly of lens
Congenital cataract
...
Disorder of anterior segment of eye
Disorder of lens
Congenital anomaly of lens
Congenital cataract
...
Disorder of anterior segment of eye
Disorder of lens
Congenital anomaly of lens
Congenital cataract
...
Disorder of anterior segment of eye
Disorder of lens
Congenital anomaly of lens
Congenital cataract
...
Congenital malformation
Congenital malformation syndrome (disorder)
Multiple system malformation syndrome
RAB18, member RAS oncogene family deficiency
...
Congenital malformation
Congenital malformation syndrome (disorder)
Multiple system malformation syndrome
RAB18, member RAS oncogene family deficiency
...
Disorder of body system
Disease of the genitourinary system
Genitourinary congenital anomalies
RAB18, member RAS oncogene family deficiency
...
Genitourinary system finding
Disease of the genitourinary system
Genitourinary congenital anomalies
RAB18, member RAS oncogene family deficiency
...
Finding of brain
Disease of brain
Congenital anomaly of brain
RAB18, member RAS oncogene family deficiency
...
Disease of the central nervous system
Disease of brain
Congenital anomaly of brain
RAB18, member RAS oncogene family deficiency
...
Disease of head
Disease of brain
Congenital anomaly of brain
RAB18, member RAS oncogene family deficiency
...
Disease of head
Disease of brain
Congenital anomaly of brain
RAB18, member RAS oncogene family deficiency
...
Disease of head
Congenital anomaly of head
Congenital anomaly of brain
RAB18, member RAS oncogene family deficiency
...
Disease of head
Congenital anomaly of head
Congenital anomaly of brain
RAB18, member RAS oncogene family deficiency
...
Congenital malformation
Congenital anomaly of head
Congenital anomaly of brain
RAB18, member RAS oncogene family deficiency
...
Congenital malformation
Congenital anomaly of head
Congenital anomaly of brain
RAB18, member RAS oncogene family deficiency
...
Disorder of eye proper (disorder)
Anomaly of eye (disorder)
Congenital anomaly of eye
RAB18, member RAS oncogene family deficiency
...
Disorder of eye proper (disorder)
Anomaly of eye (disorder)
Congenital anomaly of eye
RAB18, member RAS oncogene family deficiency
...
Disorder of eye proper (disorder)
Anomaly of eye (disorder)
Congenital anomaly of eye
RAB18, member RAS oncogene family deficiency
...
Disorder of eye proper (disorder)
Anomaly of eye (disorder)
Congenital anomaly of eye
RAB18, member RAS oncogene family deficiency
...
Disorder of eye proper (disorder)
Anomaly of eye (disorder)
Congenital anomaly of eye
RAB18, member RAS oncogene family deficiency
...
Disorder of eye proper (disorder)
Anomaly of eye (disorder)
Congenital anomaly of eye
RAB18, member RAS oncogene family deficiency
...
Disorder of eye proper (disorder)
Anomaly of eye (disorder)
Congenital anomaly of eye
RAB18, member RAS oncogene family deficiency
...
Disease of head
Congenital anomaly of head
Congenital anomaly of eye
RAB18, member RAS oncogene family deficiency
...
Disease of head
Congenital anomaly of head
Congenital anomaly of eye
RAB18, member RAS oncogene family deficiency
...
Congenital malformation
Congenital anomaly of head
Congenital anomaly of eye
RAB18, member RAS oncogene family deficiency
...
Congenital malformation
Congenital anomaly of head
Congenital anomaly of eye
RAB18, member RAS oncogene family deficiency
...
Hereditary disease
Autosomal hereditary disorder
Recessive hereditary disorder, NOS
RAB18, member RAS oncogene family deficiency
Preferred term
Warburg micro syndrome
Type
-
http://www.irandoc.ac.ir/onto/irandoc-meta/Concept
Broader concept
Associated morphology
Finding site
Is a
- 204042007
- 205681004
- Congenital cataract
- RAB18, member RAS oncogene family deficiency
Occurrence
Pathological process
In other languages
-
Persian
URI
http://www.irandoc.acir/onto/irandoc/772224009
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