Neuropathy, hereditary sensory and autonomic, type 1A

MONDO:0008086

An 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

41 clinical trials for this condition and its sub-types.

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Broader categories

Disease (618) Nervous system disorder (217) Metabolic disease (215) Hereditary disease (172) Inherited lipid metabolism disorder (165) Peripheral nervous system disorder (107) Neuromuscular disease (98) Peripheral neuropathy (90) Hereditary sensory and autonomic neuropathy (42) Inborn errors of metabolism (42)

Trials to join now! 20 Not yet recruiting 5 Not yet finished but already full! 3 Completed 13

Neuropathy, hereditary sensory and autonomic, type 1A

Broader categories

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