Hereditary sensory and autonomic neuropathy type 1
MONDO:0018213Hereditary 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
10 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome
(2)
Hereditary sensory neuropathy-deafness-dementia syndrome
(0)
Neuropathy, hereditary sensory and autonomic, type 1A
(0)
Neuropathy, hereditary sensory and autonomic, type 1C
(0)
Neuropathy, hereditary sensory, type 1D
(0)
Neuropathy, hereditary sensory, type 1F
(0)
Broader categories
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)