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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 |
|---|---|---|---|
| 1743 | DLST | dihydrolipoamide S-succinyltransferase | |
| 1946 | EFNA5 | ephrin A5 | |
| 2023 | ENO1 | enolase 1 | |
| 2026 | ENO2 | enolase 2 | |
| 2053 | EPHX2 | epoxide hydrolase 2 | |
| 2131 | EXT1 | exostosin glycosyltransferase 1 | |
| 2132 | EXT2 | exostosin glycosyltransferase 2 | |
| 2194 | FASN | fatty acid synthase | |
| 2215 | FCGR3B | Fc gamma receptor IIIb | |
| 2220 | FCN2 | ficolin 2 |
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 |
