Hereditary Sensory Autonomic Neuropathy, Type 1

Overview of Hereditary Sensory Autonomic Neuropathy, Type 1

Most recent studies have shown that Hereditary Sensory Autonomic Neuropathy, Type 1 shares some biological mechanisms with absence-of-sensation, atrophy, bone-diseases, charcot-marie-tooth-disease, foot-diseases, hereditary-sensory-and-autonomic-neuropathies, neoplasms, nervousness, neuroblastoma, pain, peripheral-neuropathy, polyneuropathy, sensory-neuropathy, sensory-neuropathy-hereditary, skin-ulcer, ulcer, weakness.

Among the many pathways, these few ones have gauged particular interests from scientists studying Hereditary Sensory Autonomic Neuropathy, Type 1, and have been seen in publications frequently: Cytokine Production, Localization, Muscle Atrophy, Reflex, Regeneration, Regulation Of Growth, Sensory Perception

Quite a number of genes have been found to play important roles in Hereditary Sensory Autonomic Neuropathy, Type 1, such as AGXT, B3GAT1, CD34, CD80, GPR151, MBOAT7, MYC, MYCN, NAA50, NGF, NINJ1, PGPEP1, PLP1, RAB7A, RAB7B, SPTLC1, SPTLC2, TAOK3. 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.

Hereditary Sensory Autonomic Neuropathy, Type 1 Related Genes

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Pathways Related to Hereditary Sensory Autonomic Neuropathy, Type 1

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

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