Managing Congenital Nephrotic Syndrome: A Guide disease
Familial Nephrotic Syndrome, also known as congenital nephrotic syndrome, is related to nephrotic syndrome, type 2 and nephrotic syndrome, type 21, and has symptoms including edema An important gene associated with Familial Nephrotic Syndrome is NPHS1 (NPHS1 Adhesion Molecule, Nephrin), and among its related pathways/superpathways are Cell ...
Understanding Congenital Mirror Movements disease
Mirror Movements 1, also known as congenital mirror movement disorder, is related to klippel-feil syndrome and melanoma. An important gene associated with Mirror Movements 1 is DCC (DCC Netrin 1 Receptor), and among its related pathways/superpathways is Regulation of commissural axon pathfinding by SLIT and ROBO. Affiliated tissues include ...
Managing Generalized Epilepsy: A Comprehensive Guide disease
Epilepsy, Idiopathic Generalized, also known as idiopathic generalized epilepsy, is related to epilepsy, idiopathic generalized 5 and generalized epilepsy with febrile seizures plus, type 7, and has symptoms including seizures, non-epileptic convulsion and absence seizures. An important gene associated with Epilepsy, Idiopathic Generalized ...
Living with Chronic Mucocutaneous Candidiasis: Tips for Care disease
Chronic Mucocutaneous Candidiasis, also known as candidiasis, chronic mucocutaneous, is related to candidiasis and immune deficiency disease, and has symptoms including scaling of skin lesions, thickening of nails and swollen periungal tissue. An important gene associated with Chronic Mucocutaneous Candidiasis is STAT1 (Signal Transducer And ...
Easing Tendinitis: Lifestyle Tips for Shoulder Health disease
Tendinitis, also known as tendinopathy, is related to patellar tendinitis and calcific tendinitis, and has symptoms including back pain, muscle cramp and sciatica. An important gene associated with Tendinitis is CRP (C-Reactive Protein), and among its related pathways/superpathways are Disease and MIF Mediated Glucocorticoid Regulation. The ...