OBO ID: DOID:0112227 |
Term Name: | tubulinopathy | Search Ontology: | |
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Definition: | A congenital nervous system abnormality characterized by complex cortical malformations including in most cases dysmorphic basal ganglia that has_material_basis_in mutation in one or more of the tubulin genes. (3) | ||
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Ontology: | Human Disease ( DOID:0112227 ) |
OTHER tubulinopathy PAGES
GENES INVOLVED
No data available
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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