MCID: AKN001
MIFTS: 21

Akinetopsia

Categories: Mental diseases

Aliases & Classifications for Akinetopsia

MalaCards integrated aliases for Akinetopsia:

Name: Akinetopsia 12 15

Classifications:



External Ids:

Disease Ontology 12 DOID:0060130

Summaries for Akinetopsia

Disease Ontology : 12 An agnosia that is a loss of motion perception.

MalaCards based summary : Akinetopsia is related to autotopagnosia and visual agnosia. An important gene associated with Akinetopsia is HNMT (Histamine N-Methyltransferase), and among its related pathways/superpathways is Sudden Infant Death Syndrome (SIDS) Susceptibility Pathways. Affiliated tissues include brain and cortex, and related phenotypes are Increased shRNA abundance (Z-score > 2) and Increased shRNA abundance (Z-score > 2)

Wikipedia : 73 Akinetopsia (Greek: a for "without", kine for "to move" and opsia for "seeing"), also known as cerebral... more...

Related Diseases for Akinetopsia

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

(show top 50) (show all 52)
# Related Disease Score Top Affiliating Genes
1 autotopagnosia 29.8 TCF20 PHC1 KLK4 HNMT
2 visual agnosia 10.3 PHC1 HNMT
3 substance-induced psychosis 10.3 TRIM32 HTR2A
4 prosopagnosia 10.2 KLK4 HNMT
5 tardive dyskinesia 10.2 HTR2A CYP2D6
6 psychosexual disorder 10.2 HTR2A CYP2D6
7 adjustment disorder 10.2 HTR2A CYP2D6
8 delusional disorder 10.2 HTR2A CYP2D6
9 coronary artery vasospasm 10.1 KNG1 HTR2A
10 high molecular weight kininogen deficiency 10.1 KNG1 KLK4
11 yemenite deaf-blind hypopigmentation syndrome 10.1
12 achromatopsia 10.1
13 form agnosia 10.0 PHC2 PHC1 HNMT GRIN1
14 appendix lymphoma 10.0 TAC1 KLK4
15 congenital nonspherocytic hemolytic anemia 10.0 KNG1 KLK4
16 oxirane allergy 10.0 KNG1 B2M
17 facial dermatosis 10.0 TAC1 KLK4
18 c1 inhibitor deficiency 10.0 KNG1 KLK4
19 perianal hematoma 10.0 TAC1 KNG1
20 interval angle-closure glaucoma 10.0 TAC1 KNG1
21 sleep disorder 10.0 TAC1 OPN4 HTR2A
22 algoneurodystrophy 10.0 TAC1 KNG1
23 pyruvate kinase deficiency of red cells 10.0 KNG1 KLK4
24 periarthritis 10.0 TAC1 B2M
25 myofascial pain syndrome 9.9 TAC1 KNG1
26 intracranial vasospasm 9.9 TAC1 KNG1
27 reflex sympathetic dystrophy 9.9 TAC1 KNG1
28 mental depression 9.9 TRIM32 OPN4 HTR2A CYP2D6
29 lingual-facial-buccal dyskinesia 9.9 HTR2A GRIN1
30 bursitis 9.9 TAC1 KNG1
31 serotonin syndrome 9.9 TAC1 HTR2A CYP2D6
32 vasomotor rhinitis 9.9 TAC1 KNG1
33 alzheimer disease 9.9
34 arteriovenous malformations of the brain 9.9
35 arteriovenous malformation 9.9
36 epilepsy 9.9
37 focal epilepsy 9.9
38 psychotic disorder 9.9 TRIM32 HTR2A CYP2D6
39 trigeminal nerve disease 9.9 TAC1 KNG1
40 specific developmental disorder 9.9 TAC1 HTR2A CYP2D6
41 nerve compression syndrome 9.9 TAC1 B2M
42 trigeminal neuralgia 9.8 TAC1 KNG1
43 agnosia 9.8 TAC1 KNG1 CYP2D6
44 acute apical periodontitis 9.8 TAC1 KNG1 CYP2D6
45 pain agnosia 9.7 TAC1 KNG1 CYP2D6
46 major depressive disorder 9.7 TAC1 OPN4 HTR2A CYP2D6
47 tendinitis 9.7 TAC1 SPP1
48 attention deficit-hyperactivity disorder 9.7 TCF20 HTR2A GRIN1 CYP2D6
49 constipation 9.7 TCF20 TAC1 CYP2D6
50 migraine with or without aura 1 9.5 TAC1 OPN4 KNG1 HTR2A CYP2D6

Graphical network of the top 20 diseases related to Akinetopsia:



Diseases related to Akinetopsia

Symptoms & Phenotypes for Akinetopsia

GenomeRNAi Phenotypes related to Akinetopsia according to GeneCards Suite gene sharing:

26 (show all 13)
# Description GenomeRNAi Source Accession Score Top Affiliating Genes
1 Increased shRNA abundance (Z-score > 2) GR00366-A-104 9.5 OPN4
2 Increased shRNA abundance (Z-score > 2) GR00366-A-115 9.5 OPN4
3 Increased shRNA abundance (Z-score > 2) GR00366-A-130 9.5 OPN4
4 Increased shRNA abundance (Z-score > 2) GR00366-A-139 9.5 OPN4
5 Increased shRNA abundance (Z-score > 2) GR00366-A-153 9.5 OPN4
6 Increased shRNA abundance (Z-score > 2) GR00366-A-165 9.5 OPN4
7 Increased shRNA abundance (Z-score > 2) GR00366-A-169 9.5 TCF20
8 Increased shRNA abundance (Z-score > 2) GR00366-A-177 9.5 TCF20
9 Increased shRNA abundance (Z-score > 2) GR00366-A-208 9.5 TCF20
10 Increased shRNA abundance (Z-score > 2) GR00366-A-212 9.5 OPN4 TCF20
11 Increased shRNA abundance (Z-score > 2) GR00366-A-4 9.5 CYP2D6 OPN4
12 Increased shRNA abundance (Z-score > 2) GR00366-A-8 9.5 TCF20
13 Increased shRNA abundance (Z-score > 2) GR00366-A-81 9.5 OPN4

Drugs & Therapeutics for Akinetopsia

Search Clinical Trials , NIH Clinical Center for Akinetopsia

Genetic Tests for Akinetopsia

Anatomical Context for Akinetopsia

MalaCards organs/tissues related to Akinetopsia:

40
Brain, Cortex

Publications for Akinetopsia

Articles related to Akinetopsia:

(show all 27)
# Title Authors PMID Year
1
The effect of target speed on perception of visual motion direction in a patient with akinetopsia. 61
30661737 2019
2
Akinetopsia on Driving. 61
31036340 2019
3
Akinetopsia with achromatopsia due to focal epilepsy. 61
30856459 2019
4
Alice in Wonderland Syndrome as a Presenting Manifestation of Creutzfeldt-Jakob Disease. 61
31143156 2019
5
The Visual Agnosias and Related Disorders. 61
28945627 2018
6
The value of cognitive neuropsychology: The case of vision research. 61
28649924 2017
7
Visual agnosia and focal brain injury. 61
28843416 2017
8
Some Unusual Neuropsychological Syndromes: Somatoparaphrenia, Akinetopsia, Reduplicative Paramnesia, Autotopagnosia. 61
27193360 2016
9
Here, there and everywhere: higher visual function and the dorsal visual stream. 61
26786007 2016
10
Neurological and neuropsychological characteristics of occipital, occipito-temporal and occipito-parietal infarction. 61
23206528 2014
11
The Zeitraffer phenomenon, akinetopsia, and the visual perception of speed of motion: a case report. 61
23557277 2014
12
Akinetopsia as epileptic seizure. 61
25667833 2013
13
Akinetopsia: acute presentation and evidence for persisting defects in motion vision. 61
21217160 2012
14
Disorders of higher visual processing. 61
21601069 2011
15
Akinetopsia in the posterior cortical variant of Alzheimer disease. 61
19720982 2009
16
Clinical management of agnosia. 61
14872395 2004
17
Disorders of motion and depth. 61
13677815 2003
18
Dog phobia in a motion-blind patient. 61
16571561 2003
19
Direction-specific motion blindness induced by focal stimulation of human extrastriate cortex. 61
12099910 2002
20
Deficits in cortical visual function. 61
11370568 2001
21
Akinetopsia from nefazodone toxicity. 61
10577608 1999
22
Spatial and temporal auditory processing deficits following right hemisphere infarction. A psychophysical study. 61
9183249 1997
23
Motion and shape perception in cerebral akinetopsia. 61
7496774 1995
24
The consequences of inactivating areas V1 and V5 on visual motion perception. 61
7895014 1995
25
The brain activity related to residual motion vision in a patient with bilateral lesions of V5. 61
7953586 1994
26
Cerebral visual motion blindness: transitory akinetopsia induced by transcranial magnetic stimulation of human area V5. 61
1360678 1992
27
Cerebral akinetopsia (visual motion blindness). A review. 61
2043951 1991

Variations for Akinetopsia

Expression for Akinetopsia

Search GEO for disease gene expression data for Akinetopsia.

Pathways for Akinetopsia

Pathways related to Akinetopsia according to GeneCards Suite gene sharing:

# Super pathways Score Top Affiliating Genes
1 11.01 TAC1 HTR2A GRIN1

GO Terms for Akinetopsia

Cellular components related to Akinetopsia according to GeneCards Suite gene sharing:

# Name GO ID Score Top Affiliating Genes
1 PcG protein complex GO:0031519 8.96 PHC2 PHC1
2 PRC1 complex GO:0035102 8.62 PHC2 PHC1

Biological processes related to Akinetopsia according to GeneCards Suite gene sharing:

# Name GO ID Score Top Affiliating Genes
1 response to steroid hormone GO:0048545 9.26 SPP1 ARG1
2 response to cadmium ion GO:0046686 9.16 B2M ARG1
3 positive regulation of cytosolic calcium ion concentration GO:0007204 9.13 TAC1 KNG1 HTR2A
4 response to amine GO:0014075 8.62 HNMT ARG1

Sources for Akinetopsia

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 ExPASy
19 FMA
20 GARD
28 GO
29 GTR
30 HMDB
31 HPO
32 ICD10
33 ICD10 via Orphanet
34 ICD9CM
35 IUPHAR
36 KEGG
37 LifeMap
39 LOVD
41 MedGen
44 MeSH
45 MESH via Orphanet
46 MGI
49 NCI
50 NCIt
51 NDF-RT
53 NINDS
54 Novoseek
56 OMIM via Orphanet
57 OMIM® (Updated 05-Apr-2021)
61 PubMed
63 QIAGEN
68 SNOMED-CT via HPO
69 Tocris
70 UMLS
71 UMLS via Orphanet
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