Down syndrome

Summary
Synonym
  • Complete trisomy 21 syndrome
  • Down's syndrome
  • Down's syndrome - trisomy 21
  • Downs syndrome
  • G Trisomy
  • trisomy 21 syndrome
Definition
A chromosomal disease that is characterized by flat-looking facial features and weak muscle tone (hypotonia) in infancy and is caused by trisomy of all or a critical portion of chromosome 21 and is associated with intellectual disability.
Super Class
chromosomal duplication syndrome
External Links
Related Genes
Displaying entries 11 - 20 of 59 in total
Gene ID Gene Symbol Description Source
929 CD14 CD14 molecule
952 CD38 CD38 molecule
1103 CHAT choline O-acetyltransferase
1312 COMT catechol-O-methyltransferase
1375 CPT1B carnitine palmitoyltransferase 1B
1555 CYP2B6 cytochrome P450 family 2 subfamily B member 6
1586 CYP17A1 cytochrome P450 family 17 subfamily A member 1
1588 CYP19A1 cytochrome P450 family 19 subfamily A member 1
2026 ENO2 enolase 2
2215 FCGR3B Fc gamma receptor IIIb
Displaying 1 entry
Gene ID Gene Symbol Description Source
80294 Pofut2 protein O-fucosyltransferase 2
Displaying 1 entry
Gene ID Gene Symbol Description Source
309686 Pofut2 protein O-fucosyltransferase 2
Displaying 1 entry
Gene ID Gene Symbol Description Source
31098 O-fut2 O-fucosyltransferase 2
Displaying 1 entry
Gene ID Gene Symbol Description Source
777668 pofut2 protein O-fucosyltransferase 2
Displaying 1 entry
Gene ID Gene Symbol Description Source Organism
779585 pofut2 protein O-fucosyltransferase 2 Xenopus tropicalis (tropical clawed frog)
Displaying 1 entry
Gene ID Gene Symbol Description Source
259529 pad-2 GDP-fucose protein O-fucosyltransferase 2

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Last updated: August 19, 2024