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Human Disease

complex cortical dysplasia with other brain malformations 6

Term ID
DOID:0090136
Synonyms
  • CDCBM56
Definition
A complex cortical dysplasia with other brain malformations that has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the tubulin beta class I (TUBB) gene on chromosome 6p21. (2)
References
Ontology
Human Disease   ( DOID:0090136 )
Relationships
is a type of
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Genes Involved
Zebrafish Models