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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 |
|---|---|---|---|
| 10400 | PEMT | phosphatidylethanolamine N-methyltransferase | |
| 10457 | GPNMB | glycoprotein nmb | |
| 10466 | COG5 | component of oligomeric golgi complex 5 | |
| 10559 | SLC35A1 | solute carrier family 35 member A1 | |
| 10724 | OGA | O-GlcNAcase | |
| 10728 | PTGES3 | prostaglandin E synthase 3 | |
| 10855 | HPSE | heparanase | |
| 10858 | CYP46A1 | cytochrome P450 family 46 subfamily A member 1 | |
| 11332 | ACOT7 | acyl-CoA thioesterase 7 | |
| 11343 | MGLL | monoglyceride lipase |
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 |
