WHIM syndrome
immunodeficiency disease characterized by neutropenia, hypogammaglobulinemia, and extensive human papillomavirus (HPV) infection. It has material basis in heterozygous mutation in the CXCR4 gene on chromosome 2q22
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WHIM syndrome
Summary
WHIM syndrome is a rare disease[1]. It has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- WHIM syndrome's instance of is recorded as rare disease[3].
- WHIM syndrome's instance of is recorded as class of disease[4].
- WHIM syndrome is a type of primary immunodeficiency disease[5].
- WHIM syndrome is a type of other immunodeficiency syndromes due to defects in innate immunity[6].
- WHIM syndrome is a type of constitutional neutropenia with extra-hematopoietic manifestations[7].
- WHIM syndrome is a type of genetic disease[8].
- WHIM syndrome is a type of autosomal dominant disease[9].
- WHIM syndrome's health specialty is recorded as immunology[10].
- WHIM syndrome's genetic association is recorded as CXCR4[11].
- WHIM syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060591[12].
- WHIM syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0060591[13].
- WHIM syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_51636[14].
- WHIM syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
Why It Matters
WHIM syndrome has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[2] It is known by 11 alternative names across languages and contexts.[16]