cognitive disorder

Summary
Synonym
  • cognitive disease
Definition
A disease of mental health that affects cognitive functions including memory processing, perception and problem solving.
Super Class
disease of mental health
Disease Ontology
DOID:1561
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
MGI genotype (from TogoID)
Related Genes
Displaying entries 1 - 10 of 21 in total
Gene ID Gene Symbol Description Source
345 APOC3 apolipoprotein C3
351 APP amyloid beta precursor protein
627 BDNF brain derived neurotrophic factor
1139 CHRNA7 cholinergic receptor nicotinic alpha 7 subunit
1312 COMT catechol-O-methyltransferase
1440 CSF3 colony stimulating factor 3
1627 DBN1 drebrin 1
1756 DMD dystrophin
2048 EPHB2 EPH receptor B2
2902 GRIN1 glutamate ionotropic receptor NMDA type subunit 1
Displaying entries 1 - 10 of 18 in total
Gene ID Gene Symbol Description Source
11441 Chrna7 cholinergic receptor, nicotinic, alpha polypeptide 7
11814 Apoc3 apolipoprotein C-III
11820 App amyloid beta precursor protein
12064 Bdnf brain derived neurotrophic factor
12846 Comt catechol-O-methyltransferase
12985 Csf3 colony stimulating factor 3 (granulocyte)
13405 Dmd dystrophin, muscular dystrophy
13844 Ephb2 Eph receptor B2
14810 Grin1 glutamate receptor, ionotropic, NMDA1 (zeta 1)
14811 Grin2a glutamate receptor, ionotropic, NMDA2A (epsilon 1)
Displaying entries 11 - 12 of 12 in total
Gene ID Gene Symbol Description Source
81687 Mmp9 matrix metallopeptidase 9
287287 Il4 interleukin 4
Displaying all 3 entries
Gene ID Gene Symbol Description Source
31002 Appl beta amyloid protein precursor-like
34304 nAChRalpha6 nicotinic Acetylcholine Receptor alpha6
40665 Nmdar1 NMDA receptor 1
Displaying all 2 entries
Gene ID Gene Symbol Description Source
561372 comta catechol-O-methyltransferase a
565370 comtb catechol-O-methyltransferase b
Displaying entry 11 - 11 of 11 in total
Gene ID Gene Symbol Description Source
191602 acr-15 Acetylcholine receptor subunit alpha-type acr-15

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Last updated: December 9, 2024