World Of Taxonomy
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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