DYX9
MCID: DYS126
MIFTS: 10

Dyslexia 9 (DYX9)

Categories: Genetic diseases, Mental diseases, Neuronal diseases

Aliases & Classifications for Dyslexia 9

MalaCards integrated aliases for Dyslexia 9:

Name: Dyslexia 9 56
Dyslexia, Susceptibility to, 9 56 13
Dyx9 56

Classifications:



External Ids:

OMIM 56 300509

Summaries for Dyslexia 9

MalaCards based summary : Dyslexia 9, also known as dyslexia, susceptibility to, 9, is related to dyslexia. An important gene associated with Dyslexia 9 is DYX9 (Dyslexia Susceptibility 9).

More information from OMIM: 300509

Related Diseases for Dyslexia 9

Diseases in the Dyslexia family:

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

Diseases related to Dyslexia 9 via text searches within MalaCards or GeneCards Suite gene sharing:

(showing 1, show less)
# Related Disease Score Top Affiliating Genes
1 dyslexia 11.5

Symptoms & Phenotypes for Dyslexia 9

Clinical features from OMIM:

300509

Drugs & Therapeutics for Dyslexia 9

Search Clinical Trials , NIH Clinical Center for Dyslexia 9

Genetic Tests for Dyslexia 9

Anatomical Context for Dyslexia 9

Publications for Dyslexia 9

Articles related to Dyslexia 9:

(showing 5, show less)
# Title Authors PMID Year
1
Genomewide scan identifies susceptibility locus for dyslexia on Xq27 in an extended Dutch family. 56
15342694 2004
2
Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia. 56
11743577 2002
3
Xq27 FRAXA locus is a strong candidate for dyslexia: evidence from a genome-wide scan in French families. 61
23307483 2013
4
The genetics of reading disability. 61
19302769 2009
5
[Genetics of dyslexia]. 61
17094062 2006

Variations for Dyslexia 9

Expression for Dyslexia 9

Search GEO for disease gene expression data for Dyslexia 9.

Pathways for Dyslexia 9

GO Terms for Dyslexia 9

Sources for Dyslexia 9

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 ExPASy
19 FMA
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
43 MeSH
44 MESH via Orphanet
45 MGI
48 NCI
49 NCIt
50 NDF-RT
53 NINDS
54 Novoseek
56 OMIM
57 OMIM via Orphanet
61 PubMed
63 QIAGEN
68 SNOMED-CT via HPO
69 TGDB
70 Tocris
71 UMLS
72 UMLS via Orphanet
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