Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

Neuropathy, hereditary sensory and autonomic, type 1C

MONDO:0013337

A hereditary sensory and autonomic neuropathy type 1 that has material basis in heterozygous mutation in the SPTLC2 gene on chromosome 14q24.

Also known as: HSAN1C, HSAN 1C, HSN 1C, hereditary sensory and autonomic neuropathy type 1C, neuropathy, hereditary sensory and autonomic, type IC, neuropathy, hereditary sensory, type 1C

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

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →
Sort by