DiGeorge syndrome

Summary
Synonym
  • 22q11.2 deletion syndrome
  • DiGeorge sequence
  • DiGeorge's syndrome
  • Pharyngeal pouch syndrome
Definition
A syndrome that has_material_basis_in a large deletion of the chromosome 22q11.2 region which includes the DGS gene needed for development of the thymus and related glands with subsequent lack of T-cell production.
Super Class
autosomal dominant disease chromosomal deletion syndrome syndrome
Related Genes
Displaying all 2 entries
Gene ID Gene Symbol Description Source
1855 DVL1 dishevelled segment polarity protein 1
7353 UFD1 ubiquitin recognition factor in ER associated degradation 1
Displaying all 7 entries
Gene ID Gene Symbol Description Source
12667 Chrd chordin
12929 Crkl v-crk avian sarcoma virus CT10 oncogene homolog-like
14179 Fgf8 fibroblast growth factor 8
15531 Ndst1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1
21813 Tgfbr2 transforming growth factor, beta receptor II
22339 Vegfa vascular endothelial growth factor A
67784 Plxnd1 plexin D1
The Human Phenotype Ontology
Displaying entries 11 - 20 of 131 in total
HPO ID HPO Term
HP:0000238 Hydrocephalus
HP:0000252 Microcephaly
HP:0000262 Turricephaly
HP:0000272 Malar flattening
HP:0000276 Long face
HP:0000286 Epicanthus
HP:0000316 Hypertelorism
HP:0000322 Short philtrum
HP:0000343 Long philtrum
HP:0000347 Micrognathia
Displaying 1 entry
Gene ID Gene Symbol Description
1312 COMT catechol-O-methyltransferase

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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: April 6, 2026