disorder of phospholipids, sphingolipids and fatty acids biosynthesis

Findings

No curated finding names disorder of phospholipids, sphingolipids and fatty acids biosynthesis yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.

Where it sits

A kind of

• inherited lipid metabolism disorder

Narrower terms (17)

• 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome
• autosomal recessive complex spastic paraplegia due to kennedy pathway dysfunction
• Barth syndrome
• congenital ichthyosis-intellectual disability-spastic quadriplegia syndrome
• fatty acid hydroxylase-associated neurodegeneration
• GM3 synthase deficiency
• hereditary sensory and autonomic neuropathy type 1
• hereditary spastic paraplegia 39
• megaconial type congenital muscular dystrophy
• nephrotic syndrome 14
• neutral lipid storage disease
• PHARC syndrome
• progressive encephalopathy with leukodystrophy due to DECR deficiency
• progressive myoclonic epilepsy type 8
• Sengers syndrome
• Sjogren-Larsson syndrome
• spinocerebellar ataxia type 38