Managing Osteogenesis Imperfecta Type VI disease
Osteogenesis Imperfecta, Type Vi, also known as osteogenesis imperfecta type 6, is related to osteogenesis imperfecta, type ii and osteogenesis imperfecta, type vii. An important gene associated with Osteogenesis Imperfecta, Type Vi is SERPINF1 (Serpin Family F Member 1), and among its related pathways/superpathways are "Platelet Aggregation ...
Understanding Enlarged Vestibular Aqueduct Syndrome disease
Deafness, Autosomal Recessive 4, with Enlarged Vestibular Aqueduct, also known as enlarged vestibular aqueduct, is related to ear malformation and pendred syndrome. An important gene associated with Deafness, Autosomal Recessive 4, with Enlarged Vestibular Aqueduct is SLC26A4 (Solute Carrier Family 26 Member 4), and among its related ...
Understanding Hereditary Paraganglioma and Lifestyle Considerations disease
Hereditary Paraganglioma-Pheochromocytoma Syndromes, also known as hereditary pheochromocytoma-paraganglioma, is related to paragangliomas 1 and sporadic pheochromocytoma/secreting paraganglioma, and has symptoms including aphonia An important gene associated with Hereditary Paraganglioma-Pheochromocytoma Syndromes is MAX (MYC Associated ...
Nighttime Asthma: Triggers and Management disease
Asthma, also known as chronic obstructive asthma, is related to allergic asthma and childhood-onset asthma, and has symptoms including recurring periods of wheezing, chest tightness and shortness of breath. An important gene associated with Asthma is IL13 (Interleukin 13), and among its related pathways/superpathways are Allograft rejection ...
Managing FSG: Lifestyle and Treatment Tips disease
Focal Segmental Glomerulosclerosis, also known as familial idiopathic steroid-resistant nephrotic syndrome, is related to focal segmental glomerulosclerosis 2 and focal segmental glomerulosclerosis 5. An important gene associated with Focal Segmental Glomerulosclerosis is NPHS1 (NPHS1 Adhesion Molecule, Nephrin), and among its related ...