OBO ID: DOID:0060401 |
Term Name: | chromosome 16q22 deletion syndrome | Search Ontology: | |
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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 | ||
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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
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