OBO ID: DOID:0060391 |
Term Name: | chromosome 13q14 deletion syndrome | Search Ontology: | |
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Definition: | A chromosomal deletion syndrome that is characterized by low birth weight, dysmorphic facies, limb defects, genital malformations and psychomotor developmental delay, has_material_basis_in deletion of the long arm of chromosome 13. https://rarediseases.org/rare-diseases/chromosome-13-partial-monosomy-13q/ | ||
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Ontology: | Human Disease ( DOID:0060391 ) |
OTHER chromosome 13q14 deletion syndrome PAGES
GENES INVOLVED
No data available
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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