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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 |
|---|---|---|---|
| 3556 | IL1RAP | interleukin 1 receptor accessory protein | |
| 3612 | IMPA1 | inositol monophosphatase 1 | |
| 3635 | INPP5D | inositol polyphosphate-5-phosphatase D | |
| 3636 | INPPL1 | inositol polyphosphate phosphatase like 1 | |
| 3707 | ITPKB | inositol-trisphosphate 3-kinase B | |
| 3821 | KLRC1 | killer cell lectin like receptor C1 | |
| 3897 | L1CAM | L1 cell adhesion molecule | |
| 3931 | LCAT | lecithin-cholesterol acyltransferase | |
| 3938 | LCT | lactase | |
| 3939 | LDHA | lactate dehydrogenase A |
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 |
