C214873Level 6
Neuropathy, Hereditary Sensory, Type IE
**Semantic type:** Disease or Syndrome
**Definition:** An autosomal dominant form of hereditary sensory neuropathy caused by mutation(s) in the DNMT1 gene encoding DNA (cytosine-5)-methyltransferase 1.
**Synonyms:** - HSN1E - Hereditary Sensory Neuropathy Type IE
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