MCID: DYS125
MIFTS: 12

Dyslexia 8

Categories: Genetic diseases, Mental diseases

Aliases & Classifications for Dyslexia 8

MalaCards integrated aliases for Dyslexia 8:

Name: Dyslexia 8 57
Dyslexia, Susceptibility to, 8 57 13
Dyx8 57

Characteristics:

OMIM:

57
Inheritance:
autosomal dominant
multifactorial



Classifications:



External Ids:

OMIM 57 608995
MedGen 42 C1837009

Summaries for Dyslexia 8

MalaCards based summary : Dyslexia 8, also known as dyslexia, susceptibility to, 8, is related to dyslexia. 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 11.2

Symptoms & Phenotypes for Dyslexia 8

Symptoms via clinical synopsis from OMIM:

57
Neurologic Central Nervous System:
dyslexia
difficulty in spelling
difficulty in phonologic coding
decreased rapid automatized naming (ran) speed


Clinical features from OMIM:

608995

Human phenotypes related to Dyslexia 8:

32
# Description HPO Frequency HPO Source Accession
1 dyslexia 32 HP:0010522

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 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 SNOMED-CT via Orphanet
71 TGDB
72 Tocris
73 UMLS
74 UMLS via Orphanet
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