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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 |
|---|---|---|---|
| 36 | ACADSB | acyl-CoA dehydrogenase short/branched chain | |
| 38 | ACAT1 | acetyl-CoA acetyltransferase 1 | |
| 217 | ALDH2 | aldehyde dehydrogenase 2 family member | |
| 410 | ARSA | arylsulfatase A | |
| 427 | ASAH1 | N-acylsphingosine amidohydrolase 1 | |
| 523 | ATP6V1A | ATPase H+ transporting V1 subunit A | |
| 847 | CAT | catalase | |
| 1103 | CHAT | choline O-acetyltransferase | |
| 1116 | CHI3L1 | chitinase 3 like 1 | |
| 1120 | CHKB | choline kinase beta |
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 |
