MCID: AST004
MIFTS: 17

Astereognosia

Categories: Eye diseases, Mental diseases

Aliases & Classifications for Astereognosia

MalaCards integrated aliases for Astereognosia:

Name: Astereognosia 12 15
Somatosensory Agnosia 12 72
Tactile Agnosia 72

Classifications:



External Ids:

Disease Ontology 12 DOID:0060150
UMLS 72 C0234505 C0459888

Summaries for Astereognosia

Disease Ontology : 12 An agnosia that is the loss of the ability to recognize objects by touch based on its texture, size and weight.

MalaCards based summary : Astereognosia, also known as somatosensory agnosia, is related to meningioma, radiation-induced and meningioma, familial, and has symptoms including visual agnosia An important gene associated with Astereognosia is CYS1 (Cystin 1). Affiliated tissues include eye, parietal lobe and cortex.

Wikipedia : 75 Astereognosis (or tactile agnosia if only one hand is affected) is the inability to identify an object... more...

Related Diseases for Astereognosia

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

(show all 11)
# Related Disease Score Top Affiliating Genes
1 meningioma, radiation-induced 10.1
2 meningioma, familial 10.1
3 agraphia 10.1
4 spinal meningioma 10.1
5 listeria meningitis 10.1
6 dysgraphia 10.1
7 secretory meningioma 10.1
8 lymphoplasmacyte-rich meningioma 10.1
9 meningitis 10.1
10 glioma 10.1
11 glial tumor 10.1

Graphical network of the top 20 diseases related to Astereognosia:



Diseases related to Astereognosia

Symptoms & Phenotypes for Astereognosia

UMLS symptoms related to Astereognosia:


visual agnosia

Drugs & Therapeutics for Astereognosia

Search Clinical Trials , NIH Clinical Center for Astereognosia

Genetic Tests for Astereognosia

Anatomical Context for Astereognosia

MalaCards organs/tissues related to Astereognosia:

41
Eye, Parietal Lobe, Cortex

Publications for Astereognosia

Articles related to Astereognosia:

(show all 16)
# Title Authors PMID Year
1
Stereoanesthesia or astereognosia? 38
19585078 2009
2
[Déjerine-Roussy syndrome of an ischaemic origin in an adolescent with patent foramen ovale]. 38
19557696 2009
3
Somatosensory and motor disturbances in patients with parietal lobe lesions. 38
12894408 2003
4
Tactile apraxia: unimodal apractic disorder of tactile object exploration associated with parietal lobe lesions. 38
11133793 2001
5
Failure to recognise objects by active touch (astereognosia) results from lesion of parietal-cortex representation of finger kinaesthesis. 38
10437873 1999
6
[Corticobasal ganglionic degeneration: a report of 7 clinically diagnosed cases]. 38
8204260 1994
7
[Congenital hemiparesis: complementary neuropsychological evaluation with computer]. 38
8147752 1993
8
Unilateral opercular macrogyria and benign childhood epilepsy with centrotemporal (rolandic) spikes: report of a case. 38
1592027 1992
9
[Cervical spondylotic myelopathies. Apropos of 121 cases. Prognostic value of sensitive symptoms]. 38
3231293 1988
10
Hemiplegic cerebral palsy. Aetiology and outcome. 38
3201989 1988
11
[Cheiro-oral syndrome with pontine infarct--report of a case]. 38
4005076 1985
12
Sequelae of transcallosal surgery. 38
7060415 1982
13
[Pure bilateral agraphia, right astereognosia and arithmetic defects associated with a left parietal tumor (author's transl)]. 38
685660 1978
14
[Pathogenesis of astereognosia and amyotrophia of the hand in superior cervical meningioma]. 38
1135550 1975
15
[Astereognosia during Listeria meningitis in an adult with a deceptive onset evoking a cerebromeningeal hemorrhage]. 38
5566779 1971
16
[On the occurrence of primary astereognosia in lesions of the cervical cord]. 38
13135430 1953

Variations for Astereognosia

Expression for Astereognosia

Search GEO for disease gene expression data for Astereognosia.

Pathways for Astereognosia

GO Terms for Astereognosia

Sources for Astereognosia

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 ExPASy
19 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 LOVD
42 MedGen
44 MeSH
45 MESH via Orphanet
46 MGI
49 NCI
50 NCIt
51 NDF-RT
54 NINDS
55 Novoseek
57 OMIM
58 OMIM via Orphanet
62 PubMed
64 QIAGEN
69 SNOMED-CT via HPO
70 TGDB
71 Tocris
72 UMLS
73 UMLS via Orphanet
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