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
Disease Ontology
DOID:11870
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
OMIM
GARD
MGI genotype (from TogoID)
Related Genes
Displaying all 8 entries
Gene ID Gene Symbol Description Source
1385 CREB1 cAMP responsive element binding protein 1
1386 ATF2 activating transcription factor 2
2353 FOS Fos proto-oncogene, AP-1 transcription factor subunit
4137 MAPT microtubule associated protein tau
5608 MAP2K6 mitogen-activated protein kinase kinase 6
6620 SNCB synuclein beta
6622 SNCA synuclein alpha
23435 TARDBP TAR DNA binding protein
Displaying all 7 entries
Gene ID Gene Symbol Description Source
11909 Atf2 activating transcription factor 2
14281 Fos FBJ osteosarcoma oncogene
17758 Map4 microtubule-associated protein 4
17762 Mapt microtubule-associated protein tau
20617 Snca synuclein, alpha
104069 Sncb synuclein, beta
140483 Hnmt histamine N-methyltransferase
Displaying all 4 entries
Gene ID Gene Symbol Description Source
29219 Snca synuclein alpha
81646 Creb1 cAMP responsive element binding protein 1
81647 Atf2 activating transcription factor 2
113893 Sncb synuclein, beta
Displaying 1 entry
Gene ID Gene Symbol Description Source
40260 Psn Presenilin
Displaying 1 entry
Gene ID Gene Symbol Description Source Organism
399258 psen1.L presenilin 1 L homeolog Xenopus laevis (African clawed frog)
Displaying 1 entry
Gene ID Gene Symbol Description Source
853313 PBS2 mitogen-activated protein kinase kinase PBS2
The Human Phenotype Ontology
Displaying entries 11 - 20 of 50 in total
HPO ID HPO Term
HP:0002145 Frontotemporal dementia
HP:0002185 Neurofibrillary tangles
HP:0002186 Apraxia
HP:0002300 Mutism
HP:0002354 Memory impairment
HP:0002366 Abnormal lower motor neuron morphology
HP:0002381 Aphasia
HP:0002427 Expressive aphasia
HP:0002446 Astrocytosis
HP:0002500 Abnormal cerebral white matter morphology
Displaying 1 entry
Gene ID Gene Symbol Description
7415 VCP valosin containing protein

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Last updated: December 9, 2024