Ether lipid biosynthesis

No Pathway Network information available for Ether lipid biosynthesis

Pathways in the Ether lipid biosynthesis SuperPath

Ordered by rank within the SuperPath, via the multiplicity of each gene in the constituent pathways

Disorders associated with Ether lipid biosynthesis SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Neonatal adrenoleukodystrophyEnrichmentPEX1, PEX16, PEX19, PEX38.61
2Peroxisome biogenesis disorder 1bEnrichmentPEX1, PEX16, PEX19, PEX38.33
3Zellweger syndromeEnrichmentPEX1, PEX16, PEX19, PEX38.33
4Rhizomelic chondrodysplasia punctataEnrichmentAGPS, GNPAT, PEX77.96
5Peroxisome biogenesis disorder 1aEnrichmentPEX1, PEX34.51
6Zellweger spectrum disorderEnrichmentPEX1, PEX194.24
7Rhizomelic chondrodysplasia punctata, type 2EnrichmentGNPAT2.83
8Peroxisome biogenesis disorder 10aEnrichmentPEX32.83
9Rhizomelic chondrodysplasia punctata, type 1EnrichmentPEX72.83
10Peroxisome biogenesis disorder 8aEnrichmentPEX162.83
11Peroxisome biogenesis disorder 12aEnrichmentPEX192.83
12Peroxisomal fatty acyl-coa reductase 1 disorderEnrichmentFAR12.83
13Peroxisome biogenesis disorder 10bEnrichmentPEX32.83
14Rhizomelic chondrodysplasia punctata, type 3EnrichmentAGPS2.83
15Majeed syndromeEnrichmentLPIN22.83
16Peroxisome biogenesis disorder 9bEnrichmentPEX72.83
17Peroxisome biogenesis disorder 8bEnrichmentPEX162.83
18Cataracts, spastic paraparesis, and speech delayEnrichmentFAR12.83
19Peroxisomal diseaseEnrichmentPEX12.83
20Autosomal recessive ataxia due to pex16 deficiencyEnrichmentPEX162.83
21Fatty acyl-coa reductase 1 deficiencyEnrichmentFAR12.83
22Myoglobinuria, acute recurrent, autosomal recessiveEnrichmentLPIN12.35
23Refsum disease, classicEnrichmentPEX72.35
24Neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset 2EnrichmentARSA2.35
25Heimler syndrome 1EnrichmentPEX12.23
26Hereditary recurrent myoglobinuriaEnrichmentLPIN12.23
27Metachromatic leukodystrophyEnrichmentARSA2.05
28LeukodystrophyEnrichmentARSA1.54
29Autoinflammatory diseaseEnrichmentLPIN21.46
30Connective tissue diseaseEnrichmentPEX71.34
31Optic atrophy plus syndromeEnrichmentPEX11.20
32Hereditary retinal dystrophyEnrichmentPEX1, PEX71.17
33Fundus dystrophyEnrichmentPEX1, PEX71.17
34Spastic ataxiaEnrichmentARSA1.12
35Congenital nervous system abnormalityEnrichmentARSA0.84
36Nervous system diseaseEnrichmentARSA0.84

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