Details of Disease | DrugMAP

General Information of Disease (ID: DISPPT30)

Disease Name	WHIM syndrome 2
Synonyms	WHIMS2
Disease Hierarchy	DIS8J18X: Whim syndrome DISPPT30: WHIM syndrome 2
Disease Identifiers	MONDO ID MONDO_0030374 UMLS CUI C5543622 OMIM ID 619407 MedGen ID 1785594

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
CXCR2	TT30C9G	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
CXCR2	OTISGW7L	Strong	Autosomal recessive	[1]
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References

1	CXCR2 deficiency confers impaired neutrophil recruitment and increased susceptibility during Toxoplasma gondii infection. J Immunol. 2001 Dec 1;167(11):6503-9. doi: 10.4049/jimmunol.167.11.6503.