Search Ontology:
Human Disease

chromosome 8q21.11 deletion syndrome

Term ID
DOID:0060425
Synonyms
  • 8q21.11 microdeletion syndrome
Definition
A chromosomal deletion syndrome that has_material_basis_in deletion of the chromosome 8q21.11 region and that is characterized by intellectual disability and common facial dysmorphic features. https://pubmed.ncbi.nlm.nih.gov/21802062/
References
Ontology
Human Disease   ( DOID:0060425 )
Relationships
is a type of
Other Pages
Alliance (1)
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.