Search Ontology:
Human Disease

periventricular nodular heterotopia 9

Term ID
DOID:0061246
Synonyms
Definition
A congenital nervous system abnormality characterized as a malformation of cortical development that has_material_basis_in heterozygous mutation in the MAP1B gene on chromosome 5q13. https://pubmed.ncbi.nlm.nih.gov/29738522/
References
Ontology
Human Disease   ( DOID:0061246 )
Relationships
Other Pages
Genes Involved
Zebrafish Models
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