Dyggve-melchior-clausen Syndrome

Overview of Dyggve-melchior-clausen Syndrome

Most recent studies have shown that Dyggve-melchior-clausen Syndrome shares some biological mechanisms with bone-diseases-developmental, chondrodysplasia-punctata, compression-of-spinal-cord, congenital-abnormality, crest-syndrome, cytogenetic-abnormality, dwarfism, dysplasia, genetic-diseases-x-linked, growth-disorders, hypoplasia, limb-deformities-congenital, microcephaly, mucopolysaccharidoses, mucopolysaccharidosis-iv, osteochondrodysplasias, shortened-trunk, skeletal-dysplasia.

Among the many pathways, these few ones have gauged particular interests from scientists studying Dyggve-melchior-clausen Syndrome, and have been seen in publications frequently: Bone Development, Endochondral Ossification, Excretion, Golgi Organization, Golgi Reassembly, Interphase, Localization, Ossification, Pathogenesis, Protein Secretion, Secretion, Transport

Quite a number of genes have been found to play important roles in Dyggve-melchior-clausen Syndrome, such as ARC, ARSH, BGN, DCN, DYM, EVC, FMOD, GLB1, GOLM1, HHIP, NOL3, PAPSS2, PPIB, PSMC1, REG3A, RPS4X, RPS4Y1, 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.

Dyggve-melchior-clausen Syndrome Related Genes

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Pathways Related to Dyggve-melchior-clausen Syndrome

This information is being compiled and will come in a future update

Related Diseases