neuropathy, hereditary sensory and autonomic, type 1C

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
neuropathy, hereditary sensory and autonomic, type 1C
SPTLC2 Causal — ClinGen
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with neuropathy, hereditary sensory and autonomic, type 1C.
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Hereditary sensory and autonomic neuropathy 1 shared geneSPTLC2 Related via 1 shared gene including SPTLC2. Charcot-marie-tooth disease 1 shared geneSPTLC2 Related via 1 shared gene including SPTLC2. Psychiatric disorders 1 shared geneSPTLC2 Related via 1 shared gene including SPTLC2. Amyotrophic lateral sclerosis 1 shared geneSPTLC2 Related via 1 shared gene including SPTLC2. Colorectal cancer 1 shared geneSPTLC2 Related via 1 shared gene including SPTLC2.