Cartilage-Hair Hypoplasia: Lifestyle and Care disease
Cartilage-Hair Hypoplasia, also known as metaphyseal chondrodysplasia, mckusick type, is related to metaphyseal dysplasia without hypotrichosis and anauxetic dysplasia 1. An important gene associated with Cartilage-Hair Hypoplasia is RMRP (RNA Component Of Mitochondrial RNA Processing Endoribonuclease), and among its related ...
Understanding Oral Mucosa Leukoplakia disease
Oral Mucosa Leukoplakia, also known as leukoplakia of buccal mucosa, is related to leukoplakia and lichen planus. An important gene associated with Oral Mucosa Leukoplakia is TEC (Tec Protein Tyrosine Kinase). The drugs Rosiglitazone and Celecoxib have been mentioned in the context of this disorder.
NKX2-5 Gene and Double Outlet Right Ventricle disease
Double Outlet Right Ventricle, also known as double outlet right ventricle with subpulmonary ventricular septal defect, is related to conotruncal heart malformations and congenital heart defects, multiple types, 6. An important gene associated with Double Outlet Right Ventricle is NKX2-5 (NK2 Homeobox 5), and among its related ...
Understanding Necrotizing Autoimmune Myopathy disease
Myopathy, Congenital, Bailey-Bloch, also known as native american myopathy, is related to malignant hyperthermia susceptibility and ptosis. An important gene associated with Myopathy, Congenital, Bailey-Bloch is STAC3 (SH3 And Cysteine Rich Domain 3), and among its related pathways/superpathways are Myometrial relaxation and contraction ...
Elevating Your Quality of Life with Peters-Plus Syndrome disease
Peters-Plus Syndrome, also known as krause-kivlin syndrome, is related to anterior segment dysgenesis 5 and intraocular pressure quantitative trait locus, and has symptoms including seizures An important gene associated with Peters-Plus Syndrome is B3GLCT (Beta 3-Glucosyltransferase), and among its related pathways/superpathways are ...