|OBO ID: DOID:0070161|
|Term Name:||hereditary sensory and autonomic neuropathy type 2||Search Ontology:|
|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|
|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
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