OBO ID: DOID:0060408 |
Term Name: | chromosome 19q13.11 deletion syndrome | Search Ontology: | |
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Definition: | A chromosomal deletion syndrome that has_material_basis_in a chromosome 19q13.11 deletion and that is characterized by characterized by poor overall growth, slender habitus, microcephaly, delayed development, intellectual disability with poor or absent speech, and feeding difficulties. https://pubmed.ncbi.nlm.nih.gov/24243649 | ||
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Ontology: | Human Disease ( DOID:0060408 ) |
OTHER chromosome 19q13.11 deletion syndrome PAGES
GENES INVOLVED
No data available
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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