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DOCK8 and stroke are reported together in 1 article.
Gene
DOCK8
- HGNC
- HGNC:19191
18articles
18mentions
0variants with confirmed gene link
Most co-reported phenotypes (articles)
Phenotype
Stroke
555articles
555mentions
12co-reported genes shown
Most co-reported genes (articles)
Counts are literature co-mentions in SaudiVarKB, not clinical or causal assertions. Gene details: HGNC; variant status: ClinVar via dbSNP.
Publications
1 records shown · first 60CNS vasculitis and stroke as a complication of DOCK8 deficiency: a case report.
PMID 27113444 | PMCID PMC4845487 | DOI 10.1186/s12883-016-0578-3 · BMC neurology · 2016 · 3 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| gene | DOCK8 | “CNS vasculitis and stroke as a complication of DOCK8 deficiency: a case report.” | 0.98 | hgnc_dict_v1 |
| phenotype | stroke | “CNS vasculitis and stroke as a complication of DOCK8 deficiency: a case report.” | 0.98 | phenotype_alias_lexicon_v2 |
| phenotype | atopic dermatitis | “Deletion of the dedicator of cytokinesis 8 (DOCK8) gene is considered to be the autosomal recessive form of hyperimmunoglobulin E syndrome which is a rare type of primary immunodeficiency disease characterized by elevated levels of IgE antibody, eczema, and recurrent staphylococcal infections.” | 0.93 | phenotype_alias_lexicon_v2 |