OBO ID: DOID:0060401
Term Name: chromosome 16q22 deletion syndrome Search Ontology:
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:
Ontology: Human Disease   ( DOID:0060401 )
OTHER chromosome 16q22 deletion syndrome PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None