MCID: FNG001
MIFTS: 16

Finger Agnosia malady

Categories: Mental diseases

Aliases & Classifications for Finger Agnosia

Aliases & Descriptions for Finger Agnosia:

Name: Finger Agnosia 12 14

Classifications:



External Ids:

Disease Ontology 12 DOID:0060141

Summaries for Finger Agnosia

Disease Ontology : 12 An agnosia that is a loss of the ability to distinguish the fingers on the hand.

MalaCards based summary : Finger Agnosia is related to gerstmann syndrome and agnosia. An important gene associated with Finger Agnosia is AGL (Amylo-Alpha-1, 6-Glucosidase, 4-Alpha-Glucanotransferase), and among its related pathways/superpathways is HIF-1 signaling pathway. Related phenotype is Decreased DCP1a protein expression and assembly in processing bodies after arsenite stimulation.

Wikipedia : 71 Finger agnosia, first defined in 1924 by Josef Gerstmann, is the loss in the ability \"to distinguish,... more...

Related Diseases for Finger Agnosia

Diseases related to Finger Agnosia via text searches within MalaCards or GeneCards Suite gene sharing:

(show all 12)
id Related Disease Score Top Affiliating Genes
1 gerstmann syndrome 11.0
2 agnosia 10.2
3 cortical deafness 9.9 EP300 MEG8
4 cytomegalovirus disease in patients with impaired cell mediated immunity deemed at risk 9.9 ENO2 MBP
5 central nervous system hemangioma 9.9 ENO2 MBP
6 adult oligodendroglioma 9.9 ENO2 MBP
7 flat ductal epithelial atypia 9.8 ENO2 MBP
8 alzheimer disease 9.7
9 agraphia 9.7
10 breast reconstruction 9.7 ENO2 MBP
11 postauricular lymphadenitis 9.5 ENO2 EP300 MBP MEG8
12 mirror agnosia 9.1 AGL CD6 ENO2 EP300 MBP MEG8

Graphical network of the top 20 diseases related to Finger Agnosia:



Diseases related to Finger Agnosia

Symptoms & Phenotypes for Finger Agnosia

GenomeRNAi Phenotypes related to Finger Agnosia according to GeneCards Suite gene sharing:

26
id Description GenomeRNAi Source Accession Score Top Affiliating Genes
1 Decreased DCP1a protein expression and assembly in processing bodies after arsenite stimulation GR00203-A 8.62 AGL EP300

Drugs & Therapeutics for Finger Agnosia

Search Clinical Trials , NIH Clinical Center for Finger Agnosia

Genetic Tests for Finger Agnosia

Anatomical Context for Finger Agnosia

Publications for Finger Agnosia

Articles related to Finger Agnosia:

id Title Authors Year
1
Clinical presentation of left angular gyrus ischaemic lesion: finger agnosia, acalculia, agraphia, left-right disorientation and episodic autoscopia. ( 23813508 )
2013
2
Finger agnosia and cognitive deficits in patients with Alzheimer's disease. ( 23373578 )
2012
3
Integration of tactile input across fingers in a patient with finger agnosia. ( 21095197 )
2011
4
Differences in finger localisation performance of patients with finger agnosia. ( 18766025 )
2008
5
Specular right-left disorientation, finger-agnosia, and asomatognosia in right hemisphere stroke. ( 17846515 )
2007
6
Finger agnosia in Alzheimer disease. ( 17159616 )
2006
7
Finger agnosia: fiction or reality? ( 8179491 )
1994
8
The unilateral forms of finger agnosia. An experimental study. ( 4760043 )
1973
9
An experimental investigation of finger agnosia. ( 5815448 )
1969
10
A study of finger agnosia. ( 14456198 )
1962

Variations for Finger Agnosia

Expression for Finger Agnosia

Search GEO for disease gene expression data for Finger Agnosia.

Pathways for Finger Agnosia

Pathways related to Finger Agnosia according to GeneCards Suite gene sharing:

id Super pathways Score Top Affiliating Genes
1 10.62 ENO2 EP300

GO Terms for Finger Agnosia

Cellular components related to Finger Agnosia according to GeneCards Suite gene sharing:

id Name GO ID Score Top Affiliating Genes
1 myelin sheath GO:0043209 8.62 ENO2 MBP

Sources for Finger Agnosia

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
16 ExPASy
18 FMA
28 GO
29 GTR
30 HGMD
31 HMDB
32 HPO
33 ICD10
34 ICD10 via Orphanet
35 ICD9CM
36 IUPHAR
37 KEGG
38 LifeMap
40 MedGen
42 MeSH
43 MESH via Orphanet
44 MGI
46 NCI
47 NCIt
48 NDF-RT
51 NINDS
52 Novoseek
54 OMIM
55 OMIM via Orphanet
59 PubMed
60 QIAGEN
65 SNOMED-CT via Orphanet
67 TGDB
68 Tocris
69 UMLS
70 UMLS via Orphanet
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