OBO ID: DOID:0060395
Term Name: chromosome 15q24 deletion syndrome Search Ontology:
Synonyms:
  • 15q24 microdeletion syndrome
Definition: A chromosomal deletion syndrome that is characterized by dysmorphic facial features, intellectual disability and seizure, has_material_basis_in autosomal dominant inheritance of mutation in the SIN3A gene causing partial deletion of the long arm of chromosome 15.https://www.omim.org/entry/613406
References:
Ontology: Human Disease   (DOID:0060395)
Relationships
is a type of:
OTHER chromosome 15q24 deletion syndrome PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
SIN3A Witteveen-Kolk syndrome 613406
ZEBRAFISH MODELSNo data available
PHENOTYPE No data available

CITATIONS: None