Concept information
...
Genetic disease
Hereditary disease
Autosomal hereditary disorder
Dominant hereditary disorder, NOS
...
Disease of brain
Congenital anomaly of brain
Congenital anomaly of cerebrum (disorder)
Cortical dysplasia
...
Disease of brain
Congenital anomaly of brain
Congenital anomaly of cerebrum (disorder)
Cortical dysplasia
...
Disease of brain
Congenital anomaly of brain
Congenital anomaly of cerebrum (disorder)
Cortical dysplasia
...
Disease of brain
Congenital anomaly of brain
Congenital anomaly of cerebrum (disorder)
Cortical dysplasia
...
Congenital anomaly of head
Congenital anomaly of brain
Congenital anomaly of cerebrum (disorder)
Cortical dysplasia
...
Congenital anomaly of head
Congenital anomaly of brain
Congenital anomaly of cerebrum (disorder)
Cortical dysplasia
Preferred term
Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation
Type
-
http://www.irandoc.ac.ir/onto/irandoc-meta/Concept
Broader concept
Associated morphology
Finding site
- 49557009
- cerebellum
- cerebral cortex
Is a
- 363070008
- 363235000
- 45163000
- Cortical dysplasia
- Dominant hereditary disorder, NOS
Occurrence
Pathological process
In other languages
URI
http://www.irandoc.acir/onto/irandoc/784344009
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