|OBO ID: DOID:0070151|
|Term Name:||hereditary sensory and autonomic neuropathy type 6||Search Ontology:|
|Definition:||A hereditary sensory neuropathy characterized by neonatal hypotonia, respiratory and feeding difficulties, impaired psychomotor development, and autonomic abnormalities that has_material_basis_in homozygous mutation in the DST gene on chromosome 6p12. https://www.ncbi.nlm.nih.gov/pubmed/22522446|
|Ontology:||Human Disease (DOID:0070151)|
|is a type of:||
OTHER hereditary sensory and autonomic neuropathy type 6 PAGES
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
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