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severe combined immunodeficiency
Summary
- Synonym
-
- SCID
- combined T and B cell inborn immunodeficiency
- Definition
- A combined T cell and B cell immunodeficiency that is caused by a defect in infection-fighting immune cells resulting in individuals with non-functional immune systems.
- Super Class
- combined immunodeficiency
External Links
- Disease Ontology
- DOID:627
- Mondo Disease Ontology
- MeSH
- UMLS
- NCI Thesaurus
- GARD
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 142 | PARP1 | poly(ADP-ribose) polymerase 1 | |
| 952 | CD38 | CD38 molecule | |
| 1048 | CEACAM5 | CEA cell adhesion molecule 5 | |
| 1087 | CEACAM7 | CEA cell adhesion molecule 7 | |
| 1573 | CYP2J2 | cytochrome P450 family 2 subfamily J member 2 | |
| 2137 | EXTL3 | exostosin like glycosyltransferase 3 | |
| 2262 | GPC5 | glypican 5 | |
| 2523 | FUT1 | fucosyltransferase 1 (H blood group) | |
| 3948 | LDHC | lactate dehydrogenase C | |
| 3956 | LGALS1 | galectin 1 |
Related Glycoprotein
