Hereditary sensory and autonomic neuropathy type II (Q84104): Difference between revisions
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Revision as of 09:28, 15 August 2026
Hereditary sensory and autonomic neuropathy, type 2 (HSAN2) is an autosomal recessive disorder characterised by profound and universal sensory loss involving large and small fibre nerves, marked hypotonia, painless fractures, trophic changes, tonic pupils, constipation, apnoeic spells.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_2016844157 |
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| English | Hereditary sensory and autonomic neuropathy type II |
Hereditary sensory and autonomic neuropathy, type 2 (HSAN2) is an autosomal recessive disorder characterised by profound and universal sensory loss involving large and small fibre nerves, marked hypotonia, painless fractures, trophic changes, tonic pupils, constipation, apnoeic spells. |
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CID11:ID_2016844157
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dki-india-ID_2016844157
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Concluído
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