Search Ontology:
Human Disease

chromosome 15q25 deletion syndrome

Term ID
DOID:0060396
Synonyms
Definition
A chromosomal deletion syndrome that is characterized by intellectual disability and developmental delay, has_material_basis_in partial deletion of the long arm of chromosome 15. https://rarediseases.info.nih.gov/diseases/10990/chromosome-15q252-microdeletion
References
Ontology
Human Disease   ( DOID:0060396 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models