Neuropathy, hereditary sensory and autonomic, type 1A

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Subtype of: Hereditary sensory and autonomic neuropathy · Neuropathy
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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 1A
MONDO:0008086
SPTLC1 Causal — ClinGen
All1 Causal1 Unknown0
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Vision loss 1 shared geneSPTLC1 Related via 1 shared gene including SPTLC1. Hsan 1 1 shared geneSPTLC1 Related via 1 shared gene including SPTLC1. Dysautonomia 1 shared geneSPTLC1 Related via 1 shared gene including SPTLC1. Macular telangiectasia 1 shared geneSPTLC1 Related via 1 shared gene including SPTLC1. Hereditary sensory and autonomic neuropathy 1 shared geneSPTLC1 Related via 1 shared gene including SPTLC1.