VSPA
MCID: SPT020
MIFTS: 15

Spatial Visualization, Aptitude for (VSPA)

Categories: Eye diseases, Neuronal diseases

Aliases & Classifications for Spatial Visualization, Aptitude for

MalaCards integrated aliases for Spatial Visualization, Aptitude for:

Name: Spatial Visualization, Aptitude for 57 70
Visuospatial/perceptual Abilities 57 13
Turner Syndrome-Associated Neurocognitive Phenotype 57
Visuospatial/perceptual Abilities; Vspa 57
Vspa 57

Characteristics:

OMIM®:

57 (Updated 05-Apr-2021)
Inheritance:
? x-linked recessive trait


HPO:

31
spatial visualization, aptitude for:
Inheritance x-linked recessive inheritance


Classifications:



External Ids:

OMIM® 57 313000
MedGen 41 C1839262
SNOMED-CT via HPO 68 88425004
UMLS 70 C1839262

Summaries for Spatial Visualization, Aptitude for

MalaCards based summary : Spatial Visualization, Aptitude for, also known as visuospatial/perceptual abilities, is related to gonadal dysgenesis and turner syndrome. An important gene associated with Spatial Visualization, Aptitude for is VSPA (Visuospatial/Perceptual Abilities). Related phenotype is abnormality of the nervous system.

More information from OMIM: 313000

Related Diseases for Spatial Visualization, Aptitude for

Diseases related to Spatial Visualization, Aptitude for via text searches within MalaCards or GeneCards Suite gene sharing:

# Related Disease Score Top Affiliating Genes
1 gonadal dysgenesis 10.1
2 turner syndrome 10.1
3 lyme disease 10.0
4 relapsing fever 10.0

Symptoms & Phenotypes for Spatial Visualization, Aptitude for

Human phenotypes related to Spatial Visualization, Aptitude for:

31
# Description HPO Frequency HPO Source Accession
1 abnormality of the nervous system 31 HP:0000707

Symptoms via clinical synopsis from OMIM®:

57 (Updated 05-Apr-2021)
Neuro:
spatial visualization aptitude

Clinical features from OMIM®:

313000 (Updated 05-Apr-2021)

Drugs & Therapeutics for Spatial Visualization, Aptitude for

Search Clinical Trials , NIH Clinical Center for Spatial Visualization, Aptitude for

Genetic Tests for Spatial Visualization, Aptitude for

Anatomical Context for Spatial Visualization, Aptitude for

Publications for Spatial Visualization, Aptitude for

Articles related to Spatial Visualization, Aptitude for:

(show all 12)
# Title Authors PMID Year
1
The Turner syndrome-associated neurocognitive phenotype maps to distal Xp. 57 61
10931762 2000
2
Genetic influences on spatial ability: transmission in an extended kindred. 57
2719626 1989
3
Familial resemblance for the Identical Blocks Test of spatial ability: no evidence for X linkage. 57
7213303 1980
4
Segregation analysis of family data for 15 tests of cognitive ability. 57
539963 1979
5
A comment on Jensen's note on sex linkage and race differences in spatial ability. 57
687314 1978
6
In pursuit of the "spatial gene": a family study. 57
637826 1978
7
A study of X chromosome linkage with field dependence and spatial visualization. 57
303515 1977
8
Spatial and temporal processing in patients with Turner's syndrome. 57
843313 1977
9
A theoretical note on sex linkage and race differences in spatial visualization ability. 57
1131144 1975
10
Further evidence of sex-linked major-gene influence on human spatial visualizing ability. 57
4684504 1973
11
Theoretical note. Sex-linked, recessive inheritance of spatial and numerical abilities, and Turner's syndrome. 57
5454128 1970
12
Girl with partial Turner syndrome and absence epilepsy. 61
18358412 2008

Variations for Spatial Visualization, Aptitude for

Expression for Spatial Visualization, Aptitude for

Search GEO for disease gene expression data for Spatial Visualization, Aptitude for.

Pathways for Spatial Visualization, Aptitude for

GO Terms for Spatial Visualization, Aptitude for

Sources for Spatial Visualization, Aptitude for

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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