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Pick's disease
Summary
- Synonym
-
- Dementia in Pick's disease
- LOBAR ATROPHY OF BRAIN
- PICK DISEASE OF BRAIN
- Pick disease
- Definition
- A frontotemporal dementia that is characterized by a spectrum of neuropsychiatric symptoms ranging from those that affect the patient's personality to those that cause a decline in cognitive function.
- Super Class
- frontotemporal dementia
External Links
- Disease Ontology
- DOID:11870
- Mondo Disease Ontology
- MeSH
- UMLS
- NCI Thesaurus
- OMIM
- GARD
- MGI genotype (from TogoID)
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 6713 | SQLE | squalene epoxidase | |
| 6900 | CNTN2 | contactin 2 | |
| 7086 | TKT | transketolase | |
| 7108 | TM7SF2 | transmembrane 7 superfamily member 2 | |
| 7167 | TPI1 | triosephosphate isomerase 1 | |
| 7355 | SLC35A2 | solute carrier family 35 member A2 | |
| 7357 | UGCG | UDP-glucose ceramide glucosyltransferase | |
| 7369 | UMOD | uromodulin | |
| 7374 | UNG | uracil DNA glycosylase | |
| 7412 | VCAM1 | vascular cell adhesion molecule 1 |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| P19320 | Vascular cell adhesion protein 1 | |
| P19367 | Hexokinase-1 | |
| P19440 | Glutathione hydrolase 1 proenzyme | |
| P20138 | Myeloid cell surface antigen CD33 | |
| P20916 | Myelin-associated glycoprotein | |
| P21399 | Cytoplasmic aconitate hydratase | |
| P21589 | 5'-nucleotidase | |
| P21964 | Catechol O-methyltransferase | |
| P22033 | Methylmalonyl-CoA mutase, mitochondrial | |
| P22303 | Acetylcholinesterase |
