Neuropathy, hereditary sensory and autonomic, type 2A
MONDO:0024309A hereditary sensory and autonomic neuropathy type 2 characterized by progressive sensory neuropathy with onset in childhood that has material basis in mutation in the HSN2 isoform of the WNK1 gene on chromosome 12p13
Also known as: HSAN 2A, HSAN2A, HSN 2A, neuropathy, hereditary sensory and autonomic, type II, neuropathy, hereditary sensory and autonomic, type IIA, neuropathy, hereditary sensory, type 2A, Morvan disease, acroosteolysis, Giaccai type
7 clinical trials for this condition and its sub-types.
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Disease
(618)
Nervous system disorder
(217)
Hereditary disease
(172)
Peripheral nervous system disorder
(107)
Neuromuscular disease
(98)
Peripheral neuropathy
(90)
Hereditary sensory and autonomic neuropathy
(42)
Human disease
(14)
Hereditary peripheral neuropathy
(6)
Hereditary neurological disease
(5)