Neuropathy, hereditary sensory and autonomic, type 1C
MONDO:0013337A hereditary sensory and autonomic neuropathy type 1 that has material basis in heterozygous mutation in the SPTLC2 gene on chromosome 14q24.
Also known as: HSAN1C, HSAN 1C, HSN 1C, hereditary sensory and autonomic neuropathy type 1C, neuropathy, hereditary sensory and autonomic, type IC, neuropathy, hereditary sensory, type 1C
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)