Aliases & Classifications for Finger Agnosia

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Aliases & Descriptions for Finger Agnosia:

Name: Finger Agnosia 10 12

Classifications:



External Ids:

Disease Ontology10 DOID:0060141

Summaries for Finger Agnosia

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Wikipedia:68 Finger agnosia, first defined in 1924 by Josef Gerstmann, is the loss in the ability \"to distinguish,... more...

MalaCards based summary: Finger Agnosia is related to gerstmann syndrome and alexander disease. An important gene associated with Finger Agnosia is AGL (Amylo-Alpha-1, 6-Glucosidase, 4-Alpha-Glucanotransferase), and among its related pathways is HIF-1 signaling pathway. Affiliated tissues include myeloid, t cells and cardiac myocytes, and related mouse phenotype respiratory system.

Disease Ontology:10 An agnosia that is a loss of the ability to distinguish the fingers on the hand.

Related Diseases for Finger Agnosia

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Graphical network of diseases related to Finger Agnosia:



Diseases related to finger agnosia

Symptoms for Finger Agnosia

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Drugs & Therapeutics for Finger Agnosia

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Interventional clinical trials:

Search ClinicalTrials, NIH Clinical Center for Finger Agnosia

Genetic Tests for Finger Agnosia

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Anatomical Context for Finger Agnosia

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MalaCards organs/tissues related to Finger Agnosia:

33
Myeloid, T cells, Cardiac myocytes

Animal Models for Finger Agnosia or affiliated genes

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MGI Mouse Phenotypes related to Finger Agnosia:

38
idDescriptionMGI Source AccessionScoreTop Affiliating Genes
1MP:00053887.8AGL, ENO2, EP300, TBX1

Publications for Finger Agnosia

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Articles related to Finger Agnosia:

idTitleAuthorsYear
1
Reconstruction of the right atrium using an extracellular matrix patch in a patient with severe mediastinal aspergillosis. (23376511)
2013
2
The C-terminal domain of Cernunnos/XLF is dispensable for DNA repair in vivo. (19103754)
2009
3
Nuclear alpha1-adrenergic receptors signal activated ERK localization to caveolae in adult cardiac myocytes. (18802028)
2008
4
Proteomic profiling identifies afamin as a potential biomarker for ovarian cancer. (18094419)
2007
5
Fluctuating hearing loss, episodic headache, and stroke with platelet hyperaggregability: coexistence of auditory neuropathy and cochlear hearing loss. (16168600)
2006
6
Varicelloviruses avoid T cell recognition by UL49.5-mediated inactivation of the transporter associated with antigen processing. (15793001)
2005
7
Histopathology of acute acalculous cholecystitis in critically ill patients. (16241996)
2005
8
Increase in systemic blood pressure during intra-arterial PD123319 infusion: evidence for functional expression of angiotensin type 2 receptors in normal volunteers. (15182114)
2004
9
Role for the mortality factors MORF4, MRGX, and MRG15 in transcriptional repression via associations with Pf1, mSin3A, and transducin-like enhancer of Split. (12391155)
2002
10
Monoclonal antibodies to the myeloid stem cells: therapeutic implications of CMA-676, a humanized anti-CD33 antibody calicheamicin conjugate. (10720144)
2000

Variations for Finger Agnosia

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Expression for genes affiliated with Finger Agnosia

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Search GEO for disease gene expression data for Finger Agnosia.

Pathways for genes affiliated with Finger Agnosia

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

idSuper pathwaysScoreTop Affiliating Genes
19.1ENO2, EP300

GO Terms for genes affiliated with Finger Agnosia

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

idNameGO IDScoreTop Affiliating Genes
1neuronal cell bodyGO:00430259.5ENO2, MBP

Biological processes related to Finger Agnosia according to GeneCards Suite gene sharing:

idNameGO IDScoreTop Affiliating Genes
1response to fatty acidGO:00705429.6EP300, MBP
2heart developmentGO:00075079.0EP300, TBX1
3cellular response to retinoic acidGO:00713009.0EP300, TBX1
4response to tumor necrosis factorGO:00346128.9EP300, MBP

Sources for Finger Agnosia

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2CDC
14ExPASy
15FDA
16FMA
24GTR
25HGMD
26HMDB
27ICD10
28ICD10 via Orphanet
29ICD9CM
30IUPHAR
31KEGG
34MedGen
36MeSH
37MESH via Orphanet
38MGI
41NCI
42NCIt
43NDF-RT
46NINDS
47Novoseek
49OMIM
50OMIM via Orphanet
54PubMed
55QIAGEN
60SNOMED-CT via Orphanet
64Tumor Gene Family of Databases
65UMLS
66UMLS via Orphanet