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bruton hypogammaglobulinemia
(phenotype)
Summary
General Info
Genetic Markers
Most Correlated Genes
Most Correlated SNPs
BTK
SH3KBP1
No SNPs found
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Pathway Enrichment
Most Correlated Biogroups
REACTOME_ANTIGEN_ACTIVATES_B_CELL_RECEPTOR_LEADING_TO_GENERATION_OF_SECOND_MESSENGERS
REACTOME_SIGNALING_BY_THE_B_CELL_RECEPTOR_BCR
SH3-like domain superfamily
SH3 domain
SH2 domain
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Curated Studies
Most Correlated Studies
Mouse Phenotypes - X-linked hereditary disease
OMIM - Congenital disorder
OMIM - Immunodeficiencies and Related Disorders
OMIM - Growth hormone deficiency
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Literature
Most Relevant Literature
First report of Wilson disease and Bruton agammaglobulinemia in the same patient caused by new mutat…
Atypical course of COVID-19 in patient with Bruton agammaglobulinemia.
Vegetative Skin Lesions in Patient with Bruton's Agammaglobulinemia.
Correction: Bruton's Agammaglobulinemia and COVID-19.
Renal amyloidosis in a patient with X-linked agammaglobulinemia (Bruton's disease) and bronchiectasi…
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Clinical Trials
Most Relevant Clinical Trials
Molecular-genetic Characterization in Patients Undergoing CAR-T Cell Infusion
A Study of LY3337641 in Rheumatoid Arthritis
Evaluation of Myoelectric Implantable Recording Array (MIRA) in Participants With Transradial Amputa…
Cortical Recording and Stimulating Array Brain-Machine Interface
Ibrutinib for the Treatment of Patients With B-Cell Malignancies Who Are Infected With Coronavirus D…
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