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Disease Info Card
Nail-patella Syndrome
Information about Nail-patella Syndrome: 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 Nail-patella Syndrome
Most recent studies have shown that Nail-patella Syndrome shares some biological mechanisms with bone-diseases-developmental, congenital-abnormality, cytogenetic-abnormality, dislocations, dysplasia, glaucoma, glaucoma-open-angle, glomerulonephritis, hereditary-diseases, hereditary-nephritis, hypoplasia, kidney-diseases, kidney-failure, kidney-failure-chronic, nails-malformed, nephritis, nephrotic-syndrome, proteinuria-of-undiagnosed-cause, renal-glomerular-disease.
Among the many pathways, these few ones have gauged particular interests from scientists studying Nail-patella Syndrome, and have been seen in publications frequently: Cell Differentiation, Cell Proliferation, Endochondral Ossification, Excretion, Eye Development, Glomerular Filtration, Kidney Development, Limb Development, Localization, Metaphase, Muscle Contraction, Nail Development, Ossification, Pathogenesis, Reflex, Renal Filtration, Translation
Quite a number of genes have been found to play important roles in Nail-patella Syndrome, such as ABL1, ABO, AK1, ASS1, CD2AP, COL4A4, COL5A1, FN1, LDB1, LDB2, LMX1B, NPHS2, NPS, NR5A1, PDLIM5, PTCH1, TCF3, TSC1. 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.