Details of Disease

General Information of Disease (ID: DISXQ4S7)

Disease Name Autism, susceptibility to, 16
Synonyms autism with or without seizures; AUTS16; susceptibility to autism 16; autism susceptibility 16; autism, susceptibility to, type 16; autism, susceptibility to, 16
Disease Hierarchy
DIS98MYE: Inherited disease susceptibility
DISRAMZ3: Autism, susceptiblity to
DISXQ4S7: Autism, susceptibility to, 16
Disease Identifiers
MONDO ID
MONDO_0013258
UMLS CUI
C3150677
OMIM ID
613410
MedGen ID
462027

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)
This Disease Is Related to 2 DTP Molecule(s)
Gene Name DTP ID Evidence Level Mode of Inheritance REF
SLC9A9 DT8LP62 Limited Autosomal dominant [1]
SLC9A9 DT8LP62 Limited Biomarker [2]
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This Disease Is Related to 1 DOT Molecule(s)
Gene Name DOT ID Evidence Level Mode of Inheritance REF
SLC9A9 OT00PCW3 Limited Autosomal dominant [1]
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References

1 Flexible and scalable diagnostic filtering of genomic variants using G2P with Ensembl VEP. Nat Commun. 2019 May 30;10(1):2373. doi: 10.1038/s41467-019-10016-3.
2 Disruption of a novel member of a sodium/hydrogen exchanger family and DOCK3 is associated with an attention deficit hyperactivity disorder-like phenotype.J Med Genet. 2003 Oct;40(10):733-40. doi: 10.1136/jmg.40.10.733.