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nervous system disease
Summary
- Definition
- A disease of anatomical entity that is located_in the central nervous system or located_in the peripheral nervous system.
- Super Class
- disease of anatomical entity
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 11343 | MGLL | monoglyceride lipase | |
| 22933 | SIRT2 | sirtuin 2 | |
| 23098 | SARM1 | sterile alpha and TIR motif containing 1 | |
| 23583 | SMUG1 | single-strand-selective monofunctional uracil-DNA glycosylase 1 | |
| 27036 | SIGLEC7 | sialic acid binding Ig like lectin 7 | |
| 27306 | HPGDS | hematopoietic prostaglandin D synthase | |
| 54732 | TMED9 | transmembrane p24 trafficking protein 9 | |
| 55512 | SMPD3 | sphingomyelin phosphodiesterase 3 | |
| 57704 | GBA2 | glucosylceramidase beta 2 | |
| 60506 | NYX | nyctalopin |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| P15289 | Arylsulfatase A | |
| P15813 | Antigen-presenting glycoprotein CD1d | |
| P15848 | Arylsulfatase B | |
| P16070 | CD44 antigen | |
| P16278 | Beta-galactosidase | |
| P16442 | Histo-blood group ABO system transferase | |
| P17050 | Alpha-N-acetylgalactosaminidase | |
| P17405 | Sphingomyelin phosphodiesterase | |
| P19367 | Hexokinase-1 | |
| P20916 | Myelin-associated glycoprotein |
