Search Ontology:
Human Disease

lissencephaly 3

Term ID
DOID:0112232
Synonyms
  • LIS3
Definition
A lissencephaly characterized by brain malformations, microcephaly, developmental delay and epilepsy that has_material_basis_in heterozygous mutation in the TUBA1A gene on chromosome 12q13.12. (2)
References
Ontology
Human Disease   ( DOID:0112232 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
Citations
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