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Standards Ontologies Notations
primary immunodeficiency disease

Summary
Synonym
  • hypoimmunity
  • immune deficiency disorder
  • immunodeficiency syndrome
Definition
An immune system disease that results when one or more essential parts of the immune system is missing or not working properly at birth due to a genetic mutation.
Super Class
immune system disease
External Links
Disease Ontology
DOID:612
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying entries 51 - 60 of 67 in total
Gene ID Gene Symbol Description Source
8809 IL18R1 interleukin 18 receptor 1
9091 PIGQ phosphatidylinositol glycan anchor biosynthesis class Q
10555 AGPAT2 1-acylglycerol-3-phosphate O-acyltransferase 2
10855 HPSE heparanase
23205 ACSBG1 acyl-CoA synthetase bubblegum family member 1
23274 CLEC16A C-type lectin domain containing 16A
23324 MAN2B2 mannosidase alpha class 2B member 2
23417 MLYCD malonyl-CoA decarboxylase
51478 HSD17B7 hydroxysteroid 17-beta dehydrogenase 7
55907 CMAS cytidine monophosphate N-acetylneuraminic acid synthetase
Displaying all 5 entries
Gene ID Gene Symbol Description Source
16195 Il6st interleukin 6 signal transducer
21897 Tlr1 toll-like receptor 1
21898 Tlr4 toll-like receptor 4
21899 Tlr6 toll-like receptor 6
24088 Tlr2 toll-like receptor 2
Displaying all 2 entries
Gene ID Gene Symbol Description Source
29260 Tlr4 toll-like receptor 4
192281 Oas1a 2'-5' oligoadenylate synthetase 1A
Displaying all 2 entries
Gene ID Gene Symbol Description Source
34137 Ostgamma Oligosaccharide transferase gamma subunit
43222 Tl Toll
Displaying 1 entry
Gene ID Gene Symbol Description Source
854252 OST3 dolichyl-diphosphooligosaccharide--protein glycotransferase OST3
Related Glycoprotein
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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: August 19, 2024