Disease Info Card

Melorheostosis

Information about Melorheostosis: characteristics, related genes and pathways, plus antibodies you can use for research. This page is being enriched constantly, if you see some information you would like this page to include please send your suggestions to us.

Overview of Melorheostosis

Most recent studies have shown that Melorheostosis shares some biological mechanisms with albers-schonberg-disease, bone-diseases, bone-diseases-developmental, congenital-abnormality, dermatofibrosis-lenticularis-disseminata, diffuse-scleroderma, dysplasia, heterotopic-ossification, hyperostosis, linear-scleroderma, localized-scleroderma, melanocytic-nevus, muscle-contracture, neoplasms, osteopoikilosis-(disorder), osteosclerosis, pain, scleroderma, sclerosis.

Among the many pathways, these few ones have gauged particular interests from scientists studying Melorheostosis, and have been seen in publications frequently: Angiogenesis, Blood Circulation, Bone Resorption, Cell Adhesion, Cell Proliferation, Innervation, Intramembranous Ossification, Localization, Muscle Atrophy, Ossification, Osteoblast Differentiation, Osteoclast Differentiation, Pathogenesis, Secretion

Quite a number of genes have been found to play important roles in Melorheostosis, such as BGLAP, C7, CXCL10, ELN, EXT1, FGF23, HHIP, LEMD3, REG3A, RPL29, RUNX2, SPARC, SS18L1, ST13, TGFB1. See what Boster has to offer for the research of these genes by clicking the gene name links below and view a more detailed info card/product listing for that gene.

In a later update, we will include information such as current drugs and therapy solutions as well as on-going and past clinical trials for this disease. Plesae stay updated.

Melorheostosis Related Genes

click to see detail information for each gene

BGLAP C7 CXCL10
ELN EXT1 FGF23
HHIP LEMD3 REG3A
RPL29 RUNX2 SPARC
SS18L1 ST13 TGFB1