| OBO ID: DOID:0060426 |
| Term Name: | chromosome 19p13.13 deletion syndrome | Search Ontology: | |
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| Definition: | A chromosomal deletion syndrome that has_material_basis_in a chromosome 19p13.13 deletion and that is characterized by an unusually large head size, tall stature, and intellectual disability that is usually moderate in severity. https://ghr.nlm.nih.gov/condition/19p1313-deletion-syndrome | ||
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| Ontology: | Human Disease ( DOID:0060426 ) |
Show first 5 Terms
OTHER chromosome 19p13.13 deletion syndrome PAGES
GENES INVOLVED
No data available
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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