Fatty acyl-CoA biosynthesis

No Pathway Network information available for Fatty acyl-CoA biosynthesis

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

Disorders associated with Fatty acyl-CoA biosynthesis SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Intellectual developmental disorder, x-linked 63EnrichmentACSL42.75
2Spinocerebellar ataxia 34EnrichmentELOVL42.75
3Ventricular tachycardia, catecholaminergic polymorphic, 3EnrichmentTECRL2.75
4Intellectual developmental disorder, autosomal recessive 14EnrichmentTECR2.75
5Congenital myopathy 11EnrichmentHACD12.75
6Diarrhea 13EnrichmentACSL52.75
7Spinocerebellar ataxia 38EnrichmentELOVL52.75
8Ichthyosis, spastic quadriplegia, and impaired intellectual developmentEnrichmentELOVL42.75
9Acetyl-coa carboxylase-alpha deficiencyEnrichmentACACA2.56
10Deafness, autosomal dominant 79EnrichmentSCD52.56
11Developmental delay, impaired growth, dysmorphic facies, and axonal neuropathyEnrichmentMORC22.56
12Charcot-marie-tooth disease, axonal, type 2zEnrichmentMORC22.56
13Stargardt disease 3EnrichmentELOVL42.45
14Combined malonic and methylmalonic aciduriaEnrichmentACSF32.45
1517-beta hydroxysteroid dehydrogenase iii deficiencyEnrichmentHSD17B32.45
16Ichthyotic keratoderma, spasticity, hypomyelination, and dysmorphic facial featuresEnrichmentELOVL12.45
17Ceroid lipofuscinosis, neuronal, 1EnrichmentPPT12.26
18Amme complexEnrichmentACSL42.15
19PseudohermaphroditismEnrichmentHSD17B32.05
20Spastic ataxiaEnrichmentELOVL4, PPT12.04
21Isolated methylmalonic acidemiaEnrichmentACSF31.91
22Catecholaminergic polymorphic ventricular tachycardiaEnrichmentTECRL1.85
23Methylmalonic acidemiaEnrichmentACSF31.85
24Difference of sex developmentEnrichmentHSD17B31.85
25Stroke, ischemicEnrichmentACSL41.76
26Epilepsy, myoclonic juvenileEnrichmentHSD17B31.71
27Neurodevelopmental disorder with dysmorphic facies and distal limb anomaliesEnrichmentPPT11.61
28Congenital myopathy 4a, autosomal dominantEnrichmentHACD11.58
29Neuronal ceroid lipofuscinosisEnrichmentPPT11.40
30Stargardt disease 1EnrichmentELOVL41.29
31Long qt syndromeEnrichmentTECRL1.27
32Non-syndromic x-linked intellectual disabilityEnrichmentACSL41.21
33Autosomal recessive non-syndromic intellectual disabilityEnrichmentTECR1.01
34Congenital nervous system abnormalityEnrichmentPPT10.60
35Nervous system diseaseEnrichmentPPT10.60
36Hereditary retinal dystrophyEnrichmentELOVL40.39
37Fundus dystrophyEnrichmentELOVL40.39
38Retinitis pigmentosaEnrichmentPPT10.35

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