DYX3
MCID: DYS122
MIFTS: 13

Dyslexia 3 (DYX3)

Categories: Genetic diseases, Mental diseases, Neuronal diseases

Aliases & Classifications for Dyslexia 3

MalaCards integrated aliases for Dyslexia 3:

Name: Dyslexia 3 57
Dyslexia, Susceptibility to, 3 57 13
Dyx3 57

Classifications:



External Ids:

OMIM® 57 604254

Summaries for Dyslexia 3

MalaCards based summary : Dyslexia 3, also known as dyslexia, susceptibility to, 3, is related to dyslexia and dyslexia 1. An important gene associated with Dyslexia 3 is DYX3 (Dyslexia Susceptibility 3).

More information from OMIM: 604254

Related Diseases for Dyslexia 3

Diseases in the Dyslexia family:

Dyslexia 1 Dyslexia 9
Dyslexia 2 Dyslexia 3
Dyslexia 6 Dyslexia 5
Dyslexia 8

Diseases related to Dyslexia 3 via text searches within MalaCards or GeneCards Suite gene sharing:

# Related Disease Score Top Affiliating Genes
1 dyslexia 11.1
2 dyslexia 1 9.9
3 dyslexia 2 9.9

Symptoms & Phenotypes for Dyslexia 3

Clinical features from OMIM®:

604254 (Updated 05-Apr-2021)

Drugs & Therapeutics for Dyslexia 3

Search Clinical Trials , NIH Clinical Center for Dyslexia 3

Genetic Tests for Dyslexia 3

Anatomical Context for Dyslexia 3

Publications for Dyslexia 3

Articles related to Dyslexia 3:

(show all 17)
# Title Authors PMID Year
1
De novo microdeletion of BCL11A is associated with severe speech sound disorder. 61 57
24810580 2014
2
Fine mapping of the 2p11 dyslexia locus and exclusion of TACR1 as a candidate gene. 61 57
15007729 2004
3
A genome scan for developmental dyslexia confirms linkage to chromosome 2p11 and suggests a new locus on 7q32. 57 61
12746395 2003
4
Supportive evidence for the DYX3 dyslexia susceptibility gene in Canadian families. 61 57
11836362 2002
5
A new gene (DYX3) for dyslexia is located on chromosome 2. 61 57
10507721 1999
6
Neural patterns of word processing differ in children with dyslexia and isolated spelling deficit. 61
33761000 2021
7
The influence of the multimedia and modality principles on the learning outcomes, satisfaction, and mental effort of college students with and without dyslexia. 61
33768387 2021
8
The Effect of Syntactic Impairment on Errors in Reading Aloud: Text Reading and Comprehension of Deaf and Hard of Hearing Children. 61
33238465 2020
9
Psychological Well-being Trajectories of Individuals with Dyslexia Aged 3-11 Years. 61
28470909 2017
10
Dyslexia and language impairment associated genetic markers influence cortical thickness and white matter in typically developing children. 61
25953057 2016
11
Genome scan for cognitive trait loci of dyslexia: Rapid naming and rapid switching of letters, numbers, and colors. 61
24807833 2014
12
A prospective genetic marker of the visual-perception disorder Meares-Irlen syndrome. 61
22913027 2012
13
A cohort of balanced reciprocal translocations associated with dyslexia: identification of two putative candidate genes at DYX1. 61
20798984 2011
14
The genetics of reading disability. 61
19302769 2009
15
A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia. 61
17309879 2007
16
Neurobiological studies of reading and reading disability. 61
11725860 2001
17
The right and wrong places to look for the cognitive locus of reading disability. 61
24235039 1988

Variations for Dyslexia 3

Expression for Dyslexia 3

Search GEO for disease gene expression data for Dyslexia 3.

Pathways for Dyslexia 3

GO Terms for Dyslexia 3

Sources for Dyslexia 3

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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