Lydia Taylor

C3 Glomerulopathy, also known as c3 glomerulonephritis, is related to glomerulonephritis and d-minus hemolytic uremic syndrome. An important gene associated with C3 Glomerulopathy is CFHR5 (Complement Factor H Related 5), and among its related pathways/superpathways are Innate Immune System and Complement cascade. The drugs Antigen-Antibody ...

Gm2-Gangliosidosis, Ab Variant, also known as hexosaminidase activator deficiency, is related to leukodystrophy and sandhoff disease, and has symptoms including hyperacusis, seizures and abnormal pyramidal signs. An important gene associated with Gm2-Gangliosidosis, Ab Variant is GM2A (Ganglioside GM2 Activator), and among its related ...

Ameloblastoma, also known as adenoameloblastoma, is related to basal cell carcinoma 1 and fibroma. An important gene associated with Ameloblastoma is AMBN (Ameloblastin), and among its related pathways/superpathways are G-Beta Gamma Signaling and Keratinization. The drugs Dabrafenib and Trametinib have been mentioned in the context of this ...

Saul-Wilson Syndrome, also known as microcephalic osteodysplastic dysplasia, saul-wilson type, is related to osteochondrodysplasia and clubfoot. An important gene associated with Saul-Wilson Syndrome is COG4 (Component Of Oligomeric Golgi Complex 4), and among its related pathways/superpathways are Vesicle-mediated transport and Golgi-to-ER ...

Fibrosis of Extraocular Muscles, Congenital, 1, also known as fibrosis of extraocular muscles, congenital, 3b, is related to moebius syndrome and fibrosis of extraocular muscles, congenital, 2, and has symptoms including cachexia, cyanosis and dyspnea. An important gene associated with Fibrosis of Extraocular Muscles, Congenital, 1 is KIF21A ...