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| Entry | Name | Description | Category | Pathway | Gene |
|---|---|---|---|---|---|
| H00097 | WHIM syndrome | WHIM (an acronym for warts, hypogammaglobulinemia, infections and myelokathexis, a form of neutropenia) syndrome is a congenital immunodeficiency disease characterized by neutropenia, hypogammaglobulinemia ... | Primary immunodeficiency |
(WHIMS1) CXCR4 [HSA:7852] [KO:K04189] (WHIMS2) CXCR2 [HSA:3579] [KO:K05050] |
| [ KEGG | DISEASE | DRUG | MEDICUS ] |