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- B093a5b567cda4428e662824ec53a31e3 hasDbXref "OMIM:619705" @default.
- B093a5b567cda4428e662824ec53a31e3 hasDbXref "https://orcid.org/0000-0002-7371-8158" @default.
- B093a5b567cda4428e662824ec53a31e3 hasDbXref "https://orcid.org/0000-0003-0113-912X" @default.
- B093a5b567cda4428e662824ec53a31e3 type Axiom @default.
- B093a5b567cda4428e662824ec53a31e3 annotatedProperty IAO_0000115 @default.
- B093a5b567cda4428e662824ec53a31e3 annotatedSource MONDO_0030528 @default.
- B093a5b567cda4428e662824ec53a31e3 annotatedTarget "An autosomal recessive disorder characterized by onset of recurrent viral and bacterial infections, particularly with encapsulated bacteria, and hypertrophic cardiomyopathy in the first months or years of life. Immunologic workup typically shows decreased circulating B cells and hypo- or agammaglobulinemia, sometimes with neutropenia or T-cell lymphocytosis, although laboratory findings may be variable among patients. Ig replacement therapy is beneficial. Cardiac involvement can also include atrial septal defect, valvular insufficiency, and pre-excitation syndrome. Rare myopathic or neurologic involvement has been reported, but these features are not consistently part of the disorder and may be related to other genetic defects." @default.