Oxytocin signaling
Pathways in the Oxytocin signaling SuperPath
| # | Name | Source | Genes |
|---|---|---|---|
| 1 | Oxytocin signaling | WikiPathways |
Ordered by rank within the SuperPath, via the multiplicity of each gene in the constituent pathways
Disorders associated with Oxytocin signaling SuperPath
according to GeneCards Suite gene sharing
| # | Disorder | Type | Genes | Score |
|---|---|---|---|---|
| 1 | Nail disorder, nonsyndromic congenital, 3 | Enrichment | PLCD1 | 3.53 |
| 2 | Sturge-weber syndrome | Enrichment | GNAQ | 3.53 |
| 3 | Qualitative or quantitative defects of caveolin-3 | Enrichment | OXTR | 3.23 |
| 4 | Phakomatosis cesioflammea | Enrichment | GNAQ | 3.23 |
| 5 | Rippling muscle disease 2 | Enrichment | OXTR | 3.05 |
| 6 | Long qt syndrome 9 | Enrichment | OXTR | 3.05 |
| 7 | Myopathy, distal, tateyama type | Enrichment | OXTR | 3.05 |
| 8 | Anastomosing haemangioma | Enrichment | GNAQ | 3.05 |
| 9 | Capillary malformations, congenital | Enrichment | GNAQ | 2.83 |
| 10 | Klippel-trenaunay-weber syndrome | Enrichment | GNAQ | 2.75 |
| 11 | Melanoma, uveal | Enrichment | GNAQ | 2.75 |
| 12 | Myopathy, tubular aggregate, 1 | Enrichment | OXTR | 2.63 |
| 13 | Creatine phosphokinase, elevated serum | Enrichment | OXTR | 2.33 |
| 14 | Isolated elevated serum creatine phosphokinase levels | Enrichment | OXTR | 2.33 |
| 15 | Cardiomyopathy, familial hypertrophic, 1 | Enrichment | OXTR | 2.15 |
| 16 | Long qt syndrome | Enrichment | OXTR | 2.04 |
| 17 | Familial hypertrophic cardiomyopathy | Enrichment | OXTR | 2.01 |
