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Human Disease

chromosome 15q24 deletion syndrome

Term ID
DOID:0060395
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
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Genes Involved
Zebrafish Models