Neuropathy, hereditary sensory, type 1F
MONDO:0014286Any hereditary sensory and autonomic neuropathy type 1 in which the cause of the disease is a mutation in the ATL3 gene.
Also known as: ATL3 hereditary sensory and autonomic neuropathy type 1, HSN1F, hereditary sensory and autonomic neuropathy type 1 caused by mutation in ATL3, neuropathy, hereditary sensory, type 1F, HSN 1F, hereditary sensory neuropathy type 1F, neuropathy, hereditary sensory, type IF
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)