Hereditary sensory and autonomic neuropathy type 1

MONDO:0018213

Hereditary sensory neuropathy type I (HSN I) is a slowly progressive neurological disorder characterized by prominent predominantly distal sensory loss, autonomic disturbances, autosomal dominant inheritance, and juvenile or adulthood disease onset.

Also known as: HSAN1, Hereditary Sensory Neuropathy Type I, hereditary sensory and autonomic neuropathy type I, HSAN 1, HSN1, hereditary sensory neuropathy type 1, neuropathy hereditary sensory and autonomic type 1, neuropathy hereditary sensory radicular, autosomal dominant

9 clinical trials for this condition and its sub-types, 0 tagged with Hereditary sensory and autonomic neuropathy type 1 itself.

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↑ Hereditary sensory and autonomic neuropathy (54) ↑ Disorder of phospholipids, sphingolipids and fatty acids biosynthesis (15)

Sub-types of Hereditary sensory and autonomic neuropathy type 1

Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome 2 trials
Hereditary sensory neuropathy-deafness-dementia syndrome 0 trials
Neuropathy, hereditary sensory and autonomic, type 1A 0 trials
Neuropathy, hereditary sensory and autonomic, type 1C 0 trials
Neuropathy, hereditary sensory, type 1D 0 trials
Neuropathy, hereditary sensory, type 1F 0 trials

Including sub-types (9) Tagged with Hereditary sensory and autonomic neuropathy type 1 (0)

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