ZFIN Human Disease: chromosome 15q24 deletion syndrome

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:	GARD:12219 ICD10CM:Q93.5 MESH:C579849 OMIM:613406 ORDO:94065
Ontology:	Human Disease ( DOID:0060395 )

Relationships

is a type of:	autosomal dominant disease chromosomal deletion syndrome autosomal dominant disease chromosomal deletion syndrome Show first 5 Terms

OTHER chromosome 15q24 deletion syndrome PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
SIN3A	sin3aa sin3ab	Witteveen-Kolk syndrome	613406

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None