Search Ontology:
Human Disease

periventricular nodular heterotopia 8

Term ID
DOID:0061245
Synonyms
Definition
A congenital nervous system abnormality characterized by abnormal neuronal migration during brain development, resulting in delayed psychomotor development that has_material_basis_in heterozygous mutation in the ARF1 gene on chromosome 1q42. https://pubmed.ncbi.nlm.nih.gov/28868155/
References
Ontology
Human Disease   ( DOID:0061245 )
Relationships
Other Pages
Genes Involved
Zebrafish Models
Your Input Welcome
We welcome your input and comments. Please use this form to recommend updates to the information in ZFIN. We appreciate as much detail as possible and references as appropriate. We will review your comments promptly.
Please check the highlighted fields and try again.
Thank you for submitting comments. Your input has been emailed to ZFIN curators who may contact you if additional information is required.
Oops. Something went wrong. Please try again later.