AUTS13
MCID: ATS375
MIFTS: 15

Autism 13 (AUTS13)

Categories: Eye diseases, Genetic diseases, Mental diseases, Neuronal diseases, Rare diseases

Aliases & Classifications for Autism 13

MalaCards integrated aliases for Autism 13:

Name: Autism 13 57
Autism Susceptibility 13 57 13
Autism, Susceptibility to, 13 57
Auts13 57

Classifications:



External Ids:

OMIM® 57 610908
OMIM Phenotypic Series 57 PS209850

Summaries for Autism 13

OMIM® : 57 Autism, the prototypic pervasive developmental disorder (PDD), is usually apparent by 3 years of age. It is characterized by a triad of limited or absent verbal communication, a lack of reciprocal social interaction or responsiveness, and restricted, stereotypic, and ritualized patterns of interests and behavior (Bailey et al., 1996; Risch et al., 1999). 'Autism spectrum disorder,' sometimes referred to as ASD, is a broader phenotype encompassing the less severe disorders Asperger syndrome (see ASPG1; 608638) and pervasive developmental disorder, not otherwise specified (PDD-NOS). 'Broad autism phenotype' includes individuals with some symptoms of autism, but who do not meet the full criteria for autism or other disorders. Mental retardation coexists in approximately two-thirds of individuals with ASD, except for Asperger syndrome, in which mental retardation is conspicuously absent (Jones et al., 2008). Genetic studies in autism often include family members with these less stringent diagnoses (Schellenberg et al., 2006). For a discussion of genetic heterogeneity of autism, see 209850. (610908) (Updated 20-May-2021)

MalaCards based summary : Autism 13, also known as autism susceptibility 13, is related to autism. An important gene associated with Autism 13 is AUTS13 (Autism, Susceptibility To, 13). Affiliated tissues include eye and brain.

Related Diseases for Autism 13

Diseases in the Autism family:

Autism 8 Autism 3
Autism 6 Autism 7
Autism 11 Autism 12
Autism 13 Autism 9
Autism 10 Autism 15
Autism 16 Autism 17
Autism 18 Autism 19
Autism 20 Autism Spectrum Disorder
Rare Disease with Autism

Diseases related to Autism 13 via text searches within MalaCards or GeneCards Suite gene sharing:

# Related Disease Score Top Affiliating Genes
1 autism 11.1

Symptoms & Phenotypes for Autism 13

Clinical features from OMIM®:

610908 (Updated 20-May-2021)

Drugs & Therapeutics for Autism 13

Search Clinical Trials , NIH Clinical Center for Autism 13

Genetic Tests for Autism 13

Anatomical Context for Autism 13

MalaCards organs/tissues related to Autism 13:

40
Eye, Brain

Publications for Autism 13

Articles related to Autism 13:

(show all 11)
# Title Authors PMID Year
1
Hypothesis: dysregulation of methylation of brain-expressed genes on the X chromosome and autism spectrum disorders. 57
18698615 2008
2
Dissecting the locus heterogeneity of autism: significant linkage to chromosome 12q14. 57
17179998 2007
3
Evidence for multiple loci from a genome scan of autism kindreds. 57
16880825 2006
4
A genomic screen of autism: evidence for a multilocus etiology. 57
10417292 1999
5
Autism: towards an integration of clinical, genetic, neuropsychological, and neurobiological perspectives. 57
8655659 1996
6
Positron emission tomography findings in children with infantile spasms and autism. 61
23219829 2013
7
Similar white matter aberrations in children with autism and their unaffected siblings: a diffusion tensor imaging study using tract-based spatial statistics. 61
20921121 2010
8
Engaging with the self: Mirror behaviour in autism, Down syndrome and typical development. 61
20841341 2010
9
Association and mutation analyses of 16p11.2 autism candidate genes. 61
19242545 2009
10
Social-cognition and the broad autism phenotype: identifying genetically meaningful phenotypes. 61
17244276 2007
11
"The frog ate the bug and made his mouth sad": narrative competence in children with autism. 61
10834770 2000

Variations for Autism 13

Expression for Autism 13

Search GEO for disease gene expression data for Autism 13.

Pathways for Autism 13

GO Terms for Autism 13

Sources for Autism 13

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 20-May-2021)
61 PubMed
63 QIAGEN
68 SNOMED-CT via HPO
69 Tocris
70 UMLS
71 UMLS via Orphanet
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