chromosome 9p deletion syndrome

Summary
Synonym
  • 9p syndrome
  • Alfi syndrome
  • monosomy 9p syndrome
Definition
A chromosomal deletion syndrome characterized by trigonocephaly, flattened occiput midface hypoplasia, long philtrum, prominent forehead, broad flat nasal bridge, anteverted nares, malformed external ears, hypertelorism, hypertonia, delayed psychomotor development and that has_material_basis_in a contiguous gene deletion on the short arm of chromosome 9.
Super Class
chromosomal deletion syndrome
Disease Ontology
DOID:0060732
Mondo Disease Ontology
MeSH
ORDO
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
158326 FREM1 FRAS1 related extracellular matrix 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
329872 Frem1 Fras1 related extracellular matrix protein 1

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024