chromosome 10q23 deletion syndrome

Term ID

DOID:0060389

Synonyms

Definition

A chromosomal deletion syndrome that is characterized by dysmorphic facies, developmental delay and multiple congenital abnormalities and huvenile polyposis, has_material_basis_in recurrent deletions of chromosome 10q22.3-q23.2. https://pubmed.ncbi.nlm.nih.gov/21248748

References

• MESH:C567385
• OMIM:612242

Ontology

Human Disease   ( DOID:0060389 )