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Entry Name Description Category Pathway Gene
H00265 Hereditary sensory and autonomic neuropathy Hereditary sensory and autonomic neuropathies (HSAN), also known as hereditary sensory neuropathies (HSN), are a clinically and genetically heterogeneous group of disorders of low prevalence. They are ... Nervous system disease hsa00600 Sphingolipid metabolism
hsa04144 Endocytosis
hsa04145 Phagosome
hsa04010 MAPK signaling pathway
hsa04210 Apoptosis
hsa04722 Neurotrophin signaling pathway
(HSAN1) SPTLC1 [HSA:10558] [KO:K00654]
(HSAN1C) SPTLC2 [HSA:9517] [KO:K00654]
(HSN1D) ATL1 [HSA:51062] [KO:K17339]
(HSN1E) DNMT1 [HSA:1786] [KO:K00558]
(HSN1F) ATL3 [HSA:25923] [KO:K17339]
(CMT2B/HMSN2B) RAB7 [HSA:7879] [KO:K07897]
(HSAN2) HSN2 [HSA:65125] [KO:K08867]
(HSAN2B) FAM134B [HSA:54463]
(HSAN2C) KIF1A [HSA:547] [KO:K10392]
(HSAN3/FD) IKBKAP [HSA:8518] [KO:K11373]
(HSAN4/CIPA) NTRK1 [HSA:4914] [KO:K03176]
(HSAN5) NGFB [HSA:4803] [KO:K02582]
(HSNSP) CCT5 [HSA:22948] [KO:K09497]
(Channelopathy associated insensitivity to pain) SCN9A [HSA:6335] [KO:K04841]
(HSAN6) DST [HSA:667] [KO:K10382]
(HSAN7) SCN11A [HSA:11280] [KO:K04843]
(HSAN8) PRDM12 [HSA:59335]
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