Neuropathy, hereditary sensory, type 1D
MONDO:0013381A hereditary sensory and autonomic neuropathy type 1 characterized by adult onset of a distal axonal sensory neuropathy that has material basis in heterozygous mutation in the ATL1 gene on chromosome 14q.
Also known as: HSN1D, hereditary sensory neuropathy type 1D, hereditary sensory neuropathy type ID, neuropathy, hereditary sensory, type ID
8 clinical trials for this condition and its sub-types.
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Disease
(680)
Metabolic disease
(233)
Nervous system disorder
(231)
Inherited lipid metabolism disorder
(189)
Hereditary disease
(176)
Peripheral nervous system disorder
(114)
Neuromuscular disease
(106)
Peripheral neuropathy
(91)
Hereditary sensory and autonomic neuropathy
(50)
Inborn errors of metabolism
(45)