chromosome 16q22 deletion syndrome

Term ID

DOID:0060401

Synonyms

Definition

A chromosomal deletion syndrome that has_material_basis_in an interstitial 16q22 deletion that is characterized by a failure to thrive in infancy, poor growth, delayed psychomotor development, hypotonia, and dysmorphic features, including large anterior fontanel, high forehead, diastasis of the cranial sutures, broad nasal bridge, hypertelorism, low-set abnormal ears, and short neck. https://www.ncbi.nlm.nih.gov/pubmed/1605249

References

• OMIM:614541

Ontology

Human Disease   ( DOID:0060401 )