Human genes for chromosome 10q23 deletion syndrome
Chromosome 10q23 deletion syndrome [DOID:0060389]
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.
Synonyms: chromosome 10q23 deletion syndrome, chromosome 10q23 deletion disease, chromosome 10q23 deletion disorder, DOID:0060389