OBO ID: DOID:0060394
Term Name: chromosome 15q13.3 microdeletion syndrome Search Ontology:
Synonyms:
  • 15q13.3 microdeletion syndrome
Definition: A chromosomal deletion syndrome that is characterized by intellectual dsability, developmental delay, autism spectrum disorder and seizure, has_material_basis_in autosomal dominant inheritance of partial deletion of the long arm of chromosome 15. https://rarediseases.info.nih.gov/diseases/10296/15q133-microdeletion-syndrome
References:
Ontology: Human Disease   ( DOID:0060394 )
Relationships
is a type of:
OTHER chromosome 15q13.3 microdeletion 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.