OBO ID: DOID:0060389
Term Name: chromosome 10q23 deletion syndrome Search Ontology:
Synonyms:
Definition: A chromosomal deletion syndrome that is characterized by dysmorphic facies, developmental delay and multiple congenital abnormalities and huvenile polyposis, has_material_basis_in recurrent deletions of chromosome 10q22.3-q23.2. https://pubmed.ncbi.nlm.nih.gov/21248748
References:
Ontology: Human Disease   ( DOID:0060389 )
Relationships
is a type of:
OTHER chromosome 10q23 deletion syndrome PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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.