Glycogen Storage Disease Ia: Symptoms and Lifestyle disease
Glycogen Storage Disease Ia, also known as glycogen storage disease type i, is related to fanconi-bickel syndrome and glycogen storage disease v, and has symptoms including intermittent diarrhea An important gene associated with Glycogen Storage Disease Ia is G6PC1 (Glucose-6-Phosphatase Catalytic Subunit 1), and among its related ...
ICF Syndrome: Management and Well-Being disease
Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome, also known as icf syndrome, is related to immunodeficiency-centromeric instability-facial anomalies syndrome 2 and immunodeficiency-centromeric instability-facial anomalies syndrome 1, and has symptoms including diarrhea An important gene associated with ...
Dietary Management for MCAD Deficiency disease
Medium-Chain Acyl-Coenzyme a Dehydrogenase Deficiency, also known as medium-chain acyl-coa dehydrogenase deficiency, is related to acyl-coa dehydrogenase, medium-chain, deficiency of and myotonia congenita, autosomal dominant, and has symptoms including lethargy, seizures and vomiting. An important gene associated with Medium-Chain ...
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 ...
Gitelman Syndrome: Managing Symptoms for Quality Life disease
Gitelman Syndrome, also known as familial hypokalemia-hypomagnesemia, is related to pseudohypoaldosteronism, type i, autosomal recessive and chondrocalcinosis, and has symptoms including muscle cramp, polyuria and seizures. An important gene associated with Gitelman Syndrome is SLC12A3 (Solute Carrier Family 12 Member 3), and among its ...