Managing X-Linked Creatine Transporter Deficiency disease
Cerebral Creatine Deficiency Syndrome 1, also known as creatine transporter deficiency, is related to cerebral creatine deficiency syndrome 3 and cerebral creatine deficiency syndrome 2, and has symptoms including constipation, muscle spasticity and seizures. An important gene associated with Cerebral Creatine Deficiency Syndrome 1 is SLC6A8 ...
Hypokalemic Periodic Paralysis: Lifestyle and Care disease
Hypokalemic Periodic Paralysis, Type 1, also known as hypokalemic periodic paralysis, is related to hypokalemic periodic paralysis, type 2 and thyrotoxic periodic paralysis, and has symptoms including muscle cramp, muscle rigidity and muscle spasticity. An important gene associated with Hypokalemic Periodic Paralysis, Type 1 is CACNA1S ...
Proctitis Management: Lifestyle and Treatment disease
Proctitis, also known as ulcerative proctitis, is related to colitis and diarrhea, and has symptoms including rectal tenesmus An important gene associated with Proctitis is EPX (Eosinophil Peroxidase), and among its related pathways/superpathways are Innate Immune System and "Clomipramine Pathway, Pharmacokinetics". The drugs Sucralfate and ...
Understanding Congenital Dysfibrinogenemia disease
Dysfibrinogenemia, Congenital, also known as dysfibrinogenemia, is related to afibrinogenemia, congenital and placental abruption. An important gene associated with Dysfibrinogenemia, Congenital is FGA (Fibrinogen Alpha Chain), and among its related pathways/superpathways are Response to elevated platelet cytosolic Ca2+ and Development ...
EBS Generalized Type: Care and Symptom Management disease
Epidermolysis Bullosa Simplex Generalized Type, also known as epidermolysis bullosa simplex, koebner type, is related to epidermolysis bullosa simplex 1b, generalized intermediate and epidermolysis bullosa simplex 1d, generalized, intermediate or severe, autosomal recessive. An important gene associated with Epidermolysis Bullosa Simplex ...