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 draws 18 Wikipedia views per month (rare_disease category, ranking #229 of 627).[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's subclass of is recorded as primary immunodeficiency disease[5].
- WHIM syndrome's subclass of is recorded as other immunodeficiency syndromes due to defects in innate immunity[6].
- WHIM syndrome's subclass of is recorded as constitutional neutropenia with extra-hematopoietic manifestations[7].
- WHIM syndrome's subclass of is recorded as genetic disease[8].
- WHIM syndrome's subclass of is recorded as autosomal dominant disease[9].
- WHIM syndrome's MeSH descriptor ID is recorded as C536697[10].
- WHIM syndrome's OMIM ID is recorded as 193670[11].
- WHIM syndrome's DiseasesDB is recorded as 32165[12].
- WHIM syndrome's Freebase ID is recorded as /m/02vqn9d[13].
- WHIM syndrome's KEGG ID is recorded as H00097[14].
- WHIM syndrome's Disease Ontology ID is recorded as DOID:0060591[15].
- WHIM syndrome's Orphanet ID is recorded as 51636[16].
- WHIM syndrome's health specialty is recorded as immunology[17].
- WHIM syndrome's genetic association is recorded as CXCR4[18].
- WHIM syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060591[19].
- WHIM syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0060591[20].
- WHIM syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_51636[21].
- WHIM syndrome's UMLS CUI is recorded as C0472817[22].
- WHIM syndrome's ICD-10-CM is recorded as D81.8[23].
- WHIM syndrome's GARD rare disease ID is recorded as 9297[24].
- WHIM syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[25].
- WHIM syndrome's Mondo ID is recorded as MONDO_0008674[26].
- WHIM syndrome's Microsoft Academic ID is recorded as 2778245530[27].
Why It Matters
WHIM syndrome draws 18 Wikipedia views per month (rare_disease category, ranking #229 of 627).[2] It has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[28] It is known by 11 alternative names across languages and contexts.[29]