MCID: SPC015
MIFTS: 9

Specific Language Impairment 4

Categories: Genetic diseases, Mental diseases

Aliases & Classifications for Specific Language Impairment 4

MalaCards integrated aliases for Specific Language Impairment 4:

Name: Specific Language Impairment 4 57 13 73
Sli4 57

Classifications:



External Ids:

OMIM 57 612514
MedGen 42 C2675874
UMLS 73 C2675874

Summaries for Specific Language Impairment 4

OMIM : 57 Vernes et al. (2008) identified polymorphisms and a haplotype within the CNTNAP2 gene (604569) on chromosome 7q35-q36 implicated in the endophenotype of nonsense word repetition as a marker of specific language impairment. (612514)

MalaCards based summary : Specific Language Impairment 4, also known as sli4, is related to specific language impairment. An important gene associated with Specific Language Impairment 4 is SLI4 (Specific Language Impairment 4).

Related Diseases for Specific Language Impairment 4

Diseases in the Specific Language Impairment family:

Specific Language Impairment 1 Specific Language Impairment 2
Specific Language Impairment 3 Specific Language Impairment 4
Specific Language Impairment 5

Diseases related to Specific Language Impairment 4 via text searches within MalaCards or GeneCards Suite gene sharing:

# Related Disease Score Top Affiliating Genes
1 specific language impairment 11.1

Symptoms & Phenotypes for Specific Language Impairment 4

Clinical features from OMIM:

612514

Drugs & Therapeutics for Specific Language Impairment 4

Search Clinical Trials , NIH Clinical Center for Specific Language Impairment 4

Genetic Tests for Specific Language Impairment 4

Anatomical Context for Specific Language Impairment 4

Publications for Specific Language Impairment 4

Variations for Specific Language Impairment 4

Expression for Specific Language Impairment 4

Search GEO for disease gene expression data for Specific Language Impairment 4.

Pathways for Specific Language Impairment 4

GO Terms for Specific Language Impairment 4

Sources for Specific Language Impairment 4

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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