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ADA and atopic dermatitis are reported together in 1 article.

Gene

ADA

HGNC
HGNC:186
4articles
4mentions
0variants with confirmed gene link
Most co-reported phenotypes (articles)
132articles
132mentions
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 60

Dupilumab for atopic manifestations in pediatric patients with inborn errors of immunity: efficacy and safety in a genetically diverse cohort.

PMID 41357247 | PMCID PMC12678239 | DOI 10.3389/fimmu.2025.1715919 · Frontiers in immunology · 2025 · 7 validated mentions
TypeEntitySource evidenceConfidenceExtractor
geneADA“RESULTS: The cohort included ten patients (6 males, 4 females) with mutations in DOCK8 (n=5), CARD11 (n=2), STAT3 LOF (n=1), ADA (n=1), and PEPD (n=1).”0.98hgnc_dict_v1
phenotypeatopic dermatitis“Severe Th2-driven atopic dermatitis and asthma are common in several IEIs, including DOCK8 deficiency, STAT3 loss-of-function, and Wiskott-Aldrich syndrome, often refractory to conventional therapies.”0.98phenotype_alias_lexicon_v2
geneDOCK8“Severe Th2-driven atopic dermatitis and asthma are common in several IEIs, including DOCK8 deficiency, STAT3 loss-of-function, and Wiskott-Aldrich syndrome, often refractory to conventional therapies.”0.98hgnc_dict_v1
geneSTAT3“Severe Th2-driven atopic dermatitis and asthma are common in several IEIs, including DOCK8 deficiency, STAT3 loss-of-function, and Wiskott-Aldrich syndrome, often refractory to conventional therapies.”0.98hgnc_dict_v1