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Hereditary sensory and autonomic neuropathy type I (HSAN I) or hereditary sensory neuropathy type I (HSN I) is a group of autosomal dominant inherited neurological diseases that affect the peripheral nervous system particularly on the sensory and autonomic functions.
A business using a part will often use a different part number than the various manufacturers of that part do. This is especially common for catalog hardware, because the same or similar part design (say, a screw with a certain standard thread, of a certain length) might be made by many corporations (as opposed to unique part designs, made by only one or a few).
Hereditary sensory and autonomic neuropathy (HSAN) or hereditary sensory neuropathy (HSN) is a condition used to describe any of the types of this disease [1] which inhibit sensation. They are less common than Charcot-Marie-Tooth disease .
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The WCO Trade Tools (WCO online database for the HS, Valuation and Origin, containing both free and paid content, with the legal text of the Harmonized System freely available) National or Regional. The US Census "Classify your Commodity" engine; Classify your Commodity video tutorial by US Census
Hereditary sensory neuropathy, type II also known as HSN2 is a region of a parent protein which in humans is encoded by the WNK1 gene. [1] [2] It is a transcript variant of the WNK1 gene that is selectively expressed in nervous system tissues, and during development.