OBO ID: DOID:0070161 |
Term Name: | hereditary sensory and autonomic neuropathy type 2 | Search Ontology: | |
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Definition: | A hereditary sensory neuropathy characterized by progressively reduced sensation to pain, temperature, and touch, loss of myelinated and unmyelinated fibers, and hypotonia with onset at birth or in early childhood. https://www.ncbi.nlm.nih.gov/pubmed/21089229 | ||
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Ontology: | Human Disease ( DOID:0070161 ) |
OTHER hereditary sensory and autonomic neuropathy type 2 PAGES
GENES INVOLVED
No data available
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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