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Up to: Inherited lipid metabolism disorder

Disorder of phospholipids, sphingolipids and fatty acids biosynthesis

0 trials tagged with this condition →

Barth syndrome 5 trials
Sjogren-Larsson syndrome 3 trials
Nephrotic syndrome 14 3 trials
Neutral lipid storage disease 1 trial · 2 incl. sub-types Sub-types →
Hereditary sensory and autonomic neuropathy type 1 0 trials · 2 incl. sub-types Sub-types →
3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome 0 trials
GM3 synthase deficiency 0 trials
PHARC syndrome 0 trials
Sengers syndrome 0 trials
Autosomal recessive complex spastic paraplegia due to kennedy pathway dysfunction 0 trials
Congenital ichthyosis-intellectual disability-spastic quadriplegia syndrome 0 trials
Fatty acid hydroxylase-associated neurodegeneration 0 trials
Hereditary spastic paraplegia 39 0 trials Sub-types →
Megaconial type congenital muscular dystrophy 0 trials
Progressive encephalopathy with leukodystrophy due to DECR deficiency 0 trials
Progressive myoclonic epilepsy type 8 0 trials
Spinocerebellar ataxia type 38 0 trials