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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
agnosia
Summary
- Synonym
-
- Dyspraxia
- Dyspraxia syndrome
- Definition
- A communication disorder that is a loss of ability to recognize objects, persons, sounds, shapes, or smells while the specific sense is not defective nor is there any significant memory loss.
- Super Class
- communication disorder
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 1203 | CLN5 | CLN5 intracellular trafficking protein | |
| 1312 | COMT | catechol-O-methyltransferase | |
| 1555 | CYP2B6 | cytochrome P450 family 2 subfamily B member 6 | |
| 1559 | CYP2C9 | cytochrome P450 family 2 subfamily C member 9 | |
| 1576 | CYP3A4 | cytochrome P450 family 3 subfamily A member 4 | |
| 1577 | CYP3A5 | cytochrome P450 family 3 subfamily A member 5 | |
| 1588 | CYP19A1 | cytochrome P450 family 19 subfamily A member 1 | |
| 1594 | CYP27B1 | cytochrome P450 family 27 subfamily B member 1 | |
| 1605 | DAG1 | dystroglycan 1 | |
| 1636 | ACE | angiotensin I converting enzyme |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q9UKY4 | Protein O-mannosyl-transferase 2 | |
| Q9UNP4 | Lactosylceramide alpha-2,3-sialyltransferase | |
| Q9UP83 | Conserved oligomeric Golgi complex subunit 5 | |
| Q9Y259 | Choline/ethanolamine kinase | |
| Q9Y487 | V-type proton ATPase 116 kDa subunit a 2 | |
| Q9Y5P6 | Mannose-1-phosphate guanyltransferase beta | |
| Q9Y6A1 | Protein O-mannosyl-transferase 1 |
