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Disease Info Card
Major Anomalies Of Jaw Size, Mandibular Hypoplasia
Information about Major Anomalies Of Jaw Size, Mandibular 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 Major Anomalies Of Jaw Size, Mandibular Hypoplasia
Most recent studies have shown that Major Anomalies Of Jaw Size, Mandibular Hypoplasia shares some biological mechanisms with airway-obstruction, apnea, cleft-palate, congenital-abnormality, congenital-small-ears, craniofacial-abnormalities, dysplasia, facial-asymmetry, fetal-growth-retardation, goldenhar-syndrome-with-ipsilateral-radial-defect, hypoplasia, malocclusion, mandibular-diseases, mandibulofacial-dysostosis, micrognathism, pierre-robin-syndrome, retrognathia, sleep-apnea-obstructive, sleep-apnea-syndromes, temporomandibular-joint-disorders.
Among the many pathways, these few ones have gauged particular interests from scientists studying Major Anomalies Of Jaw Size, Mandibular Hypoplasia, and have been seen in publications frequently: Aging, Cell Death, Cell Division, Cell Migration, Ear Development, Endochondral Ossification, Localization, Lung Development, Mastication, Mating, Neural Crest Cell Migration, Ossification, Palate Development, Pathogenesis, Pigmentation, Reflex, Regeneration, Secondary Growth, Transport, Wound Healing
Quite a number of genes have been found to play important roles in Major Anomalies Of Jaw Size, Mandibular Hypoplasia, such as CENPJ, CP, EDN1, FGF8, FUT3, GPC3, GPSM2, GYPA, GYPE, HAND2, HPS4, LMNA, MAT1A, NOG, SS18L1, ZMPSTE24. 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.