Living with Ichthyosis: Managing Symptoms and Lifestyle disease
Autosomal Recessive Congenital Ichthyosis, also known as lamellar ichthyosis, is related to ichthyosis, congenital, autosomal recessive 1 and ichthyosis, congenital, autosomal recessive 2. An important gene associated with Autosomal Recessive Congenital Ichthyosis is ALOX12B (Arachidonate 12-Lipoxygenase, 12R Type), and among its related ...
Managing Congenital Stationary Night Blindness disease
Congenital Stationary Night Blindness, also known as night blindness, congenital stationary, is related to night blindness, congenital stationary, type 1a and x-linked congenital stationary night blindness. An important gene associated with Congenital Stationary Night Blindness is NYX (Nyctalopin), and among its related ...
Manage Primary Congenital Glaucoma with Healthy Habits disease
Glaucoma 3, Primary Congenital, a, also known as buphthalmos, is related to gillespie syndrome and aniridia 1, and has symptoms including early vision loss An important gene associated with Glaucoma 3, Primary Congenital, a is CYP1B1 (Cytochrome P450 Family 1 Subfamily B Member 1), and among its related pathways/superpathways are Diseases of ...
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 ...
Understanding Congenital Sodium Diarrhea disease
Diarrhea 3, Secretory Sodium, Congenital, with or Without Other Congenital Anomalies, also known as diarrhea 3, secretory sodium, congenital, syndromic, is related to diarrhea 8, secretory sodium, congenital and diarrhea, and has symptoms including diarrhea and watery diarrhea. An important gene associated with Diarrhea 3, Secretory Sodium, ...