Details of Disease

General Information of Disease (ID: DIS4CNXL)

Disease Name Autism, susceptibility to, 19
Synonyms AUTS19; susceptibility to autism 19; autism, susceptibility to, type 19; autism, susceptibility to, 19
Definition Not listed in the OMIM series but the page directs you to 209850 for the full details.
Disease Hierarchy
DIS98MYE: Inherited disease susceptibility
DISRAMZ3: Autism, susceptiblity to
DIS4CNXL: Autism, susceptibility to, 19
Disease Identifiers
MONDO ID
MONDO_0014041
UMLS CUI
C3554495
OMIM ID
615091
MedGen ID
767409

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)
This Disease Is Related to 1 DTT Molecule(s)
Gene Name DTT ID Evidence Level Mode of Inheritance REF
EIF4E TTZGCP6 Limited Unknown [1]
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This Disease Is Related to 1 DOT Molecule(s)
Gene Name DOT ID Evidence Level Mode of Inheritance REF
EIF4E OTDAWNLA Limited Unknown [1]
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References

1 Deregulation of EIF4E: a novel mechanism for autism. J Med Genet. 2009 Nov;46(11):759-65. doi: 10.1136/jmg.2009.066852. Epub 2009 Jun 25.