Estrogen metabolism

No Pathway Network information available for Estrogen metabolism

Pathways in the Estrogen metabolism SuperPath

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

Disorders associated with Estrogen metabolism SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Crigler-najjar syndrome, type iEnrichmentUGT1A1, UGT1A3, UGT1A6, UGT1A99.35
2Hyperbilirubinemia, transient familial neonatalEnrichmentUGT1A1, UGT1A3, UGT1A6, UGT1A99.35
3Bilirubin, serum level of, quantitative trait locus 1EnrichmentUGT1A1, UGT1A3, UGT1A6, UGT1A99.35
4Crigler-najjar syndrome, type iiEnrichmentUGT1A1, UGT1A3, UGT1A6, UGT1A99.35
5Gilbert syndromeEnrichmentUGT1A1, UGT1A3, UGT1A6, UGT1A99.14
6Bilirubin metabolic disorderEnrichmentUGT1A1, UGT1A3, UGT1A6, UGT1A99.14
7Chondrodysplasia punctata, brachytelephalangic, autosomalEnrichmentARSL2.88
8Chondrodysplasia punctata 1, x-linked recessiveEnrichmentARSL2.88
9Vitamin d-dependent rickets, type 3EnrichmentCYP3A42.88
10X-linked chondrodysplasia punctata 1EnrichmentARSL2.88
11Catechol-o-methyltransferase activity, variation inEnrichmentCOMT2.88
12Syndromic recessive x-linked ichthyosisEnrichmentSTS2.88
13Glaucoma 1, open angle, aEnrichmentCYP1B12.58
14Anterior segment dysgenesis 6EnrichmentCYP1B12.58
15Ichthyosis, x-linkedEnrichmentSTS2.58
16Primary congenital glaucomaEnrichmentCYP1B12.58
17Glaucoma 3, primary infantile, bEnrichmentCYP1B12.28
18Juvenile glaucomaEnrichmentCYP1B12.18
19Glaucoma, primary open angleEnrichmentCYP1B12.10
20Anterior segment dysgenesis 5EnrichmentCYP1B12.10
21Glaucoma 3, primary congenital, aEnrichmentCYP1B12.03
22Peters-plus syndromeEnrichmentCYP1B11.88
23Digeorge syndromeEnrichmentCOMT1.80
24Coffin-siris syndrome 1EnrichmentARSL1.70
25Anterior segment dysgenesisEnrichmentCYP1B11.70
26Bardet-biedl syndromeEnrichmentCOMT1.27
27SchizophreniaEnrichmentCOMT1.12

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