Antley-bixler Syndrome, Autosomal Dominant

Overview of Antley-bixler Syndrome, Autosomal Dominant

Most recent studies have shown that Antley-bixler Syndrome, Autosomal Dominant shares some biological mechanisms with adrenal-hyperplasia, ambiguous-genitalia, atresia, brachycephaly, choanal-atresia, congenital-abnormal-synostosis, congenital-abnormality, congenital-adrenal-hyperplasia, craniofacial-abnormalities, craniosynostosis, dysplasia, fracture, hyperplasia, hypoplasia, muscle-contracture, por-deficiency, stenosis, virilism.

Among the many pathways, these few ones have gauged particular interests from scientists studying Antley-bixler Syndrome, Autosomal Dominant, and have been seen in publications frequently: Cholesterol Homeostasis, Excretion, Heart Development, Localization, Ossification, Pathogenesis, Vasculogenesis

Quite a number of genes have been found to play important roles in Antley-bixler Syndrome, Autosomal Dominant, such as BRCA2, CYB5A, CYCS, CYP17A1, CYP19A1, CYP21A2, CYP51A1, DDX41, FANCD2, FGFR2, FMN1, POMC, POR, PORCN, PSEN1, SHH, VDAC2. See what Boster has to offer for the research of these genes by clicking the gene name links below and view a more detailed info card/product listing for that gene.

In a later update, we will include information such as current drugs and therapy solutions as well as on-going and past clinical trials for this disease. Plesae stay updated.

Antley-bixler Syndrome, Autosomal Dominant Related Genes

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Pathways Related to Antley-bixler Syndrome, Autosomal Dominant

This information is being compiled and will come in a future update

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