ZFIN Human Disease: chromosome 15q25 deletion syndrome

OBO ID: DOID:0060396

OBO ID: DOID:0060396

Term Name:	chromosome 15q25 deletion syndrome	Search Ontology:
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:	OMIM:614294
Ontology:	Human Disease ( DOID:0060396 )

Relationships

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

OTHER chromosome 15q25 deletion syndrome PAGES

Alliance (1)

GENES INVOLVED No data available

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None