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

7 clinical trials for this condition and its sub-types, 0 tagged with Neuropathy, hereditary sensory and autonomic, type 1A itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Hereditary sensory and autonomic neuropathy type 1 (2)

Including sub-types (7) Tagged with Neuropathy, hereditary sensory and autonomic, type 1A (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.