DYX8
MCID: DYS125
MIFTS: 13

Dyslexia 8 (DYX8)

Categories: Genetic diseases, Mental diseases

Aliases & Classifications for Dyslexia 8

MalaCards integrated aliases for Dyslexia 8:

Name: Dyslexia 8 58
Dyslexia, Susceptibility to, 8 58 13
Dyx8 58

Characteristics:

OMIM:

58
Inheritance:
autosomal dominant
multifactorial



Classifications:



External Ids:

OMIM 58 608995
MedGen 43 C1837009

Summaries for Dyslexia 8

MalaCards based summary : Dyslexia 8, also known as dyslexia, susceptibility to, 8, is related to dyslexia and perrault syndrome 1. An important gene associated with Dyslexia 8 is DYX8 (Dyslexia Susceptibility 8). Related phenotype is dyslexia.

Description from OMIM: 608995

Related Diseases for Dyslexia 8

Diseases in the Dyslexia family:

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

Diseases related to Dyslexia 8 via text searches within MalaCards or GeneCards Suite gene sharing:

# Related Disease Score Top Affiliating Genes
1 dyslexia 11.3
2 perrault syndrome 1 11.1

Symptoms & Phenotypes for Dyslexia 8

Human phenotypes related to Dyslexia 8:

33
# Description HPO Frequency HPO Source Accession
1 dyslexia 33 HP:0010522

Symptoms via clinical synopsis from OMIM:

58
Neurologic Central Nervous System:
dyslexia
difficulty in spelling
difficulty in phonologic coding
decreased rapid automatized naming (ran) speed

Clinical features from OMIM:

608995

Drugs & Therapeutics for Dyslexia 8

Search Clinical Trials , NIH Clinical Center for Dyslexia 8

Genetic Tests for Dyslexia 8

Anatomical Context for Dyslexia 8

Publications for Dyslexia 8

Variations for Dyslexia 8

Expression for Dyslexia 8

Search GEO for disease gene expression data for Dyslexia 8.

Pathways for Dyslexia 8

GO Terms for Dyslexia 8

Sources for Dyslexia 8

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 ExPASy
20 FMA
29 GO
30 GTR
31 HGMD
32 HMDB
33 HPO
34 ICD10
35 ICD10 via Orphanet
36 ICD9CM
37 IUPHAR
38 KEGG
39 LifeMap
41 LOVD
43 MedGen
45 MeSH
46 MESH via Orphanet
47 MGI
50 NCI
51 NCIt
52 NDF-RT
55 NINDS
56 Novoseek
58 OMIM
59 OMIM via Orphanet
63 PubMed
65 QIAGEN
70 SNOMED-CT via HPO
71 SNOMED-CT via Orphanet
72 TGDB
73 Tocris
74 UMLS
75 UMLS via Orphanet
Content
Loading form....