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WormBase Tree Display for DO_term: DOID:0070156

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Name Class

DOID:0070156Namehereditary sensory neuropathy type 1D
StatusValid
DefinitionA hereditary sensory and autonomic neuropathy type 1 characterized dult onset of a distal axonal sensory neuropathy affecting all modalities, often associated with distal ulceration and amputation as well as hyporeflexia, although some patients may show features suggesting upper neuron involvement that has_material_basis_in heterozygous mutation in the ATL1 gene on chromosome 14q.
SynonymExactHSN1D
ParentIs_aDOID:0050736
DOID:0070162
DB_infoDatabaseOMIMdisease613708
Attribute_ofGene_by_orthologyWBGene00021868