Neuropathy, hereditary sensory and autonomic, type 1A
MONDO:0008086An axonal form of hereditary motor and sensory neuropathy distinguished by prominent early sensory loss and later positive sensory phenomena, caused by mutations in SPTLC1.
Also known as: HSAN1A, SPTLC1 hereditary sensory and autonomic neuropathy type 1, hereditary sensory and autonomic neuropathy type 1 caused by mutation in SPTLC1, HSAN 1A, HSN 1A, hereditary sensory and autonomic neuropathy type 1A, neuropathy, hereditary sensory and autonomic, type IA, neuropathy, hereditary sensory radicular, autosomal dominant, type 1A
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)