Bisphosphonate Pathway, Pharmacodynamics

No Pathway Network information available for Bisphosphonate Pathway, Pharmacodynamics

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

Disorders associated with Bisphosphonate Pathway, Pharmacodynamics SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Noonan syndrome 1EnrichmentHRAS, KRAS, MRAS, NRAS, RRAS10.17
2Schimmelpenning-feuerstein-mims syndromeEnrichmentHRAS, KRAS, NRAS8.67
3Nevus, epidermalEnrichmentHRAS, KRAS, NRAS7.73
4RasopathyEnrichmentHRAS, KRAS, MRAS, NRAS7.61
5Lung non-small cell carcinomaEnrichmentHRAS, KRAS, NRAS7.06
6Noonan syndrome and noonan-related syndromeEnrichmentHRAS, KRAS, NRAS6.62
7Juvenile myelomonocytic leukemiaEnrichmentKRAS, NRAS, RRAS6.45
8Ras-associated autoimmune leukoproliferative disorderEnrichmentKRAS, NRAS6.14
9Differentiated thyroid carcinomaEnrichmentHRAS, KRAS, NRAS5.72
10Large congenital melanocytic nevusEnrichmentHRAS, NRAS5.67
11Chronic myelogenous leukemia, bcr-abl1 positiveEnrichmentKRAS, NRAS5.37
12Thyroid cancer, nonmedullary, 2EnrichmentHRAS, NRAS4.82
13Leukemia, chronic myeloidEnrichmentKRAS, NRAS4.82
14Noonan syndrome 3EnrichmentHRAS, KRAS4.82
15Follicular thyroid carcinomaEnrichmentHRAS, NRAS4.82
16Melanocytic nevus syndrome, congenitalEnrichmentHRAS, NRAS4.70
17Bladder cancerEnrichmentHRAS, KRAS3.54
18Non-immune hydrops fetalisEnrichmentHRAS, KRAS3.48
19Leukemia, acute myeloidEnrichmentKRAS, NRAS3.26
20Oculoectodermal syndromeEnrichmentKRAS3.05
21Immunodeficiency 73a with defective neutrophil chemotaxis and leukocytosisEnrichmentRAC23.05
22Melanosis, neurocutaneousEnrichmentNRAS3.05
23Noonan syndrome 6EnrichmentNRAS3.05
24Hiatt-neu-cooper neurodevelopmental syndromeEnrichmentRALA3.05
25Neurodevelopmental disorder with structural brain anomalies and dysmorphic faciesEnrichmentRAC33.05
26Immunodeficiency 73c with defective neutrophil chemotaxis and hypogammaglobulinemiaEnrichmentRAC23.05
27Cardiofaciocutaneous syndrome 2EnrichmentKRAS3.05
28Takenouchi-kosaki syndromeEnrichmentCDC423.05
29Neurodevelopmental disorder with microcephaly, seizures, and brain atrophyEnrichmentEXOC83.05
30Immunodeficiency 73b with defective neutrophil chemotaxis and lymphopeniaEnrichmentRAC23.05
31Congenital pulmonary airway malformationEnrichmentKRAS3.05
32Infantile lad-like disease due to rac2 deficiencyEnrichmentRAC23.05
33Reticular dysgenesis-like severe combined immunodeficiencyEnrichmentRAC23.05
34Nocarh syndromeEnrichmentCDC423.05
35Phakomatosis pigmentokeratoticaEnrichmentHRAS3.05
36Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndromEnrichmentRAC13.05
37Rac2-related combined immunodeficiency-bronchiectasis-cancer-predisposing syndromeEnrichmentRAC23.05
38Neurocutaneous melanocytosisEnrichmentNRAS3.05
39Noonan syndrome 11EnrichmentMRAS2.90
40Ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomaliesEnrichmentRHOA2.90
41Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomaliesEnrichmentRHOA2.90
42Low density lipoprotein cholesterol level quantitative trait locus 3EnrichmentHMGCR2.90
43Muscular dystrophy, limb-girdle, autosomal recessive 28EnrichmentHMGCR2.90
44Costello syndromeEnrichmentHRAS2.75
45Encephalocraniocutaneous lipomatosisEnrichmentKRAS2.75
46Intellectual developmental disorder, autosomal dominant 48EnrichmentRAC12.75
47Immune system diseaseEnrichmentCDC422.75
48Neurodevelopmental disorder with dysmorphic facies and cerebellar hypoplasiaEnrichmentEXOC22.75
49Wooly hair nevusEnrichmentHRAS2.75
50Squalene synthase deficiencyEnrichmentFDFT12.60
51Porokeratosis 9, multiple typesEnrichmentFDPS2.60
52Langerhans cell histiocytosisEnrichmentNRAS2.58
53SpermatocytomaEnrichmentHRAS2.58
54Cardiofaciocutaneous syndrome 1EnrichmentKRAS2.45
55Diffuse gastric and lobular breast cancer syndromeEnrichmentKRAS2.45
56Cardiofaciocutaneous syndromeEnrichmentKRAS2.45
57Lung sarcomatoid carcinomaEnrichmentKRAS2.45
58Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemiaEnrichmentCDC422.45
59Pilocytic astrocytomaEnrichmentKRAS2.45
60Epidermolytic nevusEnrichmentHRAS2.45
61PorokeratosisEnrichmentFDPS2.30
62Complex neurodevelopmental disorderEnrichmentRAC3, RALA2.29
63Breast adenocarcinomaEnrichmentKRAS2.28
64Lung squamous cell carcinomaEnrichmentKRAS2.28
65Capillary malformation-arteriovenous malformation 1EnrichmentKRAS2.21
66Gallbladder cancerEnrichmentKRAS2.21
67Pilomyxoid astrocytomaEnrichmentKRAS2.21
68Congenital myopathy 3 with rigid spineEnrichmentHMGCS12.20
69Hemihyperplasia, isolatedEnrichmentRHOA2.13
70Neurodevelopmental disorder with dysmorphic facies and distal limb anomaliesEnrichmentRAC12.10
71Arteriovenous malformationEnrichmentHRAS2.10
72Myopathy, x-linked, with excessive autophagyEnrichmentHRAS2.05
73Lip and oral cavity carcinomaEnrichmentHRAS1.98
74Limb-girdle muscular dystrophyEnrichmentHMGCR1.95
75Protein-deficiency anemiaEnrichmentNRAS1.94
76Lung cancer susceptibility 3EnrichmentKRAS1.91
77Lynch syndromeEnrichmentKRAS1.88
78RhabdomyosarcomaEnrichmentHRAS1.85
79Arteriovenous malformations of the brainEnrichmentKRAS1.78
80Pancreatic cancerEnrichmentKRAS1.66
81Hydrops fetalis, nonimmuneEnrichmentHRAS1.64
82Lung cancerEnrichmentKRAS1.55
83Gastric cancerEnrichmentKRAS1.43
84Hereditary breast carcinomaEnrichmentKRAS1.42
85Hereditary breast ovarian cancer syndromeEnrichmentKRAS1.32
86Myeloma, multipleEnrichmentKRAS1.31
87Breast cancerEnrichmentKRAS1.19
88Colorectal cancerEnrichmentNRAS1.13
89Ovarian cancerEnrichmentKRAS1.07

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