neuropathy, hereditary sensory, type 1D

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
neuropathy, hereditary sensory, type 1D
ATL1 Causal — ClinGen —
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with neuropathy, hereditary sensory, type 1D.
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Potassium deficiency 1 shared geneATL1 Related via 1 shared gene including ATL1. Hereditary sensory and autonomic neuropathy 1 shared geneATL1 Related via 1 shared gene including ATL1. Dupuytren contracture 1 shared geneATL1 Related via 1 shared gene including ATL1. Hereditary spastic paraplegia 1 shared geneATL1 Related via 1 shared gene including ATL1. Congenital neurologic anomalies 1 shared geneATL1 Related via 1 shared gene including ATL1.