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Disease Info Card
Micromelia
Information about Micromelia: 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 Micromelia
Most recent studies have shown that Micromelia shares some biological mechanisms with achondroplasia, bone-diseases-developmental, cleft-palate, congenital-abnormality, dwarfism, dysplasia, edema, fetal-death, fetal-diseases, growth-retardation, hydrocephalus, hypoplasia, limb-deformities-congenital, micrognathism, osteochondrodysplasias, polydactyly, short-rib-polydactyly-syndrome, skeletal-dysplasia, teratogenic-effect.
Among the many pathways, these few ones have gauged particular interests from scientists studying Micromelia, and have been seen in publications frequently: Bone Maturation, Brain Development, Cartilage Development, Cell Adhesion, Cell Death, Cell Migration, Cell Proliferation, Constitutive Secretory Pathway, Endochondral Ossification, Excretion, Limb Development, Limb Morphogenesis, Localization, Ossification, Pathogenesis, Regeneration, Secretion, Secretory Pathway, Transport, Transposition
Quite a number of genes have been found to play important roles in Micromelia, such as ACAN, ACHE, BAG6, COL2A1, DCN, ERMAP, FGFR3, IK, INS, PTH, PTRH1, SLC25A12, SLC26A2, SS18L1. 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.