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Disease Info Card
Cartilage Hair Hypoplasia
Information about Cartilage Hair Hypoplasia: 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 Cartilage Hair Hypoplasia
Most recent studies have shown that Cartilage Hair Hypoplasia shares some biological mechanisms with achondroplasia, anemia, bone-diseases-developmental, cartilage-diseases, congenital-combined-immunodeficiency, dwarfism, dysplasia, hair-diseases, hirschsprung-disease, hypoplasia, immunologic-deficiency-syndromes, infective-disorder, lymphopenia, malignant-neoplasms, metaphyseal-chondrodysplasia, osteochondrodysplasias, pyle-metaphyseal-dysplasia, severe-combined-immunodeficiency, skeletal-dysplasia.
Among the many pathways, these few ones have gauged particular interests from scientists studying Cartilage Hair Hypoplasia, and have been seen in publications frequently: Aging, Bone Maturation, Cell Cycle, Cell Growth, Cell Proliferation, Chondrocyte Hypertrophy, Excretion, Hypersensitivity, Immune Response, Localization, Lymphocyte Proliferation, Mitochondrial Rna Processing, Mitosis, Mrna Cleavage, Oxidative Phosphorylation, Pathogenesis, Plasma Cell Differentiation, Ribosome Assembly, Ribosome Biogenesis, Rna Processing
Quite a number of genes have been found to play important roles in Cartilage Hair Hypoplasia, such as ABCC1, ADA, CCNB2, COL10A1, GH1, IL2, IL2RA, LBR, MARCKSL1, MTSS1, RPS19, RSAD2, SOD2, WLS. 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.