Signaling by Retinoic Acid

No Pathway Network information available for Signaling by Retinoic Acid

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

Disorders associated with Signaling by Retinoic Acid SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Pyruvate dehydrogenase e1-alpha deficiencyEnrichmentPDHA1, PDHX4.27
2Diaphragmatic hernia 4, with cardiovascular defectsEnrichmentALDH1A22.79
3Radiohumeral fusions with other skeletal and craniofacial anomaliesEnrichmentCYP26B12.79
4Focal facial dermal dysplasia 4EnrichmentCYP26C12.79
5Lethal occipital encephalocele-skeletal dysplasia syndromeEnrichmentCYP26B12.79
6MicrophthalmiaEnrichmentALDH1A3, RARB2.70
7Charcot-marie-tooth disease, x-linked dominant, 6EnrichmentPDK32.52
8Microphthalmia, syndromic 12EnrichmentRARB2.52
9Spermatogenic failure 70EnrichmentPDHA22.52
10Retinal dystrophy, juvenile cataracts, and short stature syndromeEnrichmentRDH112.49
11Microphthalmia, isolated 8EnrichmentALDH1A32.49
12Isolated anophthalmia-microphthalmia syndromeEnrichmentALDH1A32.31
13Dihydrolipoamide dehydrogenase deficiencyEnrichmentDLD2.22
14Methemoglobinemia due to deficiency of methemoglobin reductaseEnrichmentDLD2.22
15Pyruvate dehydrogenase e2 deficiencyEnrichmentDLAT2.22
16Pyruvate dehydrogenase e1-beta deficiencyEnrichmentPDHB2.22
17Pyruvate dehydrogenase e3-binding protein deficiencyEnrichmentPDHX2.22
18Intellectual developmental disorder, autosomal dominant 48EnrichmentRARB2.22
19Parkinson disease, mitochondrialEnrichmentADH1C2.19
20Alcohol dependenceEnrichmentADH1C2.01
21Fundus albipunctatusEnrichmentRDH51.95
22Spermatogenic failure 1EnrichmentPDHA21.92
23NanophthalmosEnrichmentALDH1A31.75
24Macs syndromeEnrichmentALDH1A31.50
25Lactic acidosisEnrichmentDLD1.45
26Congenital stationary night blindnessEnrichmentRDH51.44
27Parkinson disease, late-onsetEnrichmentADH1C1.42
28Microphthalmia/coloboma 12EnrichmentRARB1.41
29Acute promyelocytic leukemiaEnrichmentRARA1.41
30Coloboma of maculaEnrichmentRARB1.35
31Sudden infant death syndromeEnrichmentPDHA11.30
32AzoospermiaEnrichmentPDHA21.23
33Optic atrophy plus syndromeEnrichmentRDH51.16
34Hereditary retinal dystrophyEnrichmentRDH11, RDH51.10
35Fundus dystrophyEnrichmentRDH11, RDH51.10
36AutismEnrichmentALDH1A30.96
37Myeloma, multipleEnrichmentRXRA0.81
38Male infertility with azoospermia or oligozoospermia due to single gene mutationEnrichmentPDHA20.81
39Mitochondrial diseaseEnrichmentPDHX0.63
40Retinitis pigmentosaEnrichmentRDH50.53

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