Details of Disease | DrugMAP

General Information of Disease (ID: DISDL1RW)

Disease Name	Hatipoglu immunodeficiency syndrome
Disease Hierarchy	DIS093I0: Immunodeficiency DISDL1RW: Hatipoglu immunodeficiency syndrome
Disease Identifiers	MONDO ID MONDO_0957229 UMLS CUI C5830439 OMIM ID 620331 MedGen ID 1841075

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
DPP9	TTNDUL7	Strong	Autosomal recessive	[1]
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This Disease Is Related to 1 DOT Molecule(s)

Gene Name	DOT ID	Evidence Level	Mode of Inheritance	REF
DPP9	OTBMZW2O	Strong	Autosomal recessive	[1]
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References

1	Prevalence and architecture of de novo mutations in developmental disorders. Nature. 2017 Feb 23;542(7642):433-438. doi: 10.1038/nature21062. Epub 2017 Jan 25.