WormBase Tree Display for DO_term: DOID:0070156
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DOID:0070156 | Name | hereditary sensory neuropathy type 1D | |||
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Status | Valid | ||||
Definition | A 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. | ||||
Synonym | Exact | HSN1D | |||
Parent | Is_a | DOID:0050736 | |||
DOID:0070162 | |||||
DB_info | Database | OMIM | disease | 613708 | |
Attribute_of | Gene_by_orthology | WBGene00021868 |