Hereditary spastic paraplegia 39

MONDO:0012787

This syndrome is characterized by progressive spastic paraplegia and distal muscle wasting.

Also known as: NTE-related motor neuron disorder, NTEMND, PNPLA6 hereditary spastic paraplegia, SPG39, autosomal recessive spastic paraplegia type 39, hereditary spastic paraplegia caused by mutation in PNPLA6, hereditary spastic paraplegia type 39, spastic paraplegia due to NTE mutation

2 clinical trials for this condition and its sub-types, 0 tagged with Hereditary spastic paraplegia 39 itself.

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↑ Syndromic dyslipidemia (73) ↑ Disorder of phospholipids, sphingolipids and fatty acids biosynthesis (15) ↑ Complex hereditary spastic paraplegia (7)

Sub-types of Hereditary spastic paraplegia 39

PNPLA6-related spastic paraplegia with or without ataxia 0 trials

Including sub-types (2) Tagged with Hereditary spastic paraplegia 39 (0)

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