Cutis Laxa, X-linked

Overview of Cutis Laxa, X-linked

Most recent studies have shown that Cutis Laxa, X-linked shares some biological mechanisms with aneurysm, atrophy, connective-tissue-diseases, copper-deficiency, copper-metabolism-disorder, cutis-laxa, diverticulum, ehlers-danlos-syndrome, exostoses, hepatolenticular-degeneration, hereditary-diseases, menkes-kinky-hair-syndrome, nerve-degeneration, nervousness, neurodegenerative-disorders, peripheral-motor-neuropathy.

Among the many pathways, these few ones have gauged particular interests from scientists studying Cutis Laxa, X-linked, and have been seen in publications frequently: Aging, Brain Development, Endoplasmic Reticulum Localization, Golgi Localization, Localization, Methylation, Mrna Processing, Mrna Splicing, Muscle Atrophy, Secretion, Translation, Transport, Wound Healing

Quite a number of genes have been found to play important roles in Cutis Laxa, X-linked, such as ATOX1, ATP7A, BRD2, CP, DBH, EIF4G2, ELN, GDF10, HSPA5, LOX, PRB1, PSMD2, QPCT, TG, VCP. 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.

Cutis Laxa, X-linked Related Genes

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Pathways Related to Cutis Laxa, X-linked

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

Related Diseases