Signaling by BMP

Pathway network for the Signaling by BMP SuperPath

Sources:
  • Reactome
  • PubChem

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

Disorders associated with Signaling by BMP SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Heritable pulmonary arterial hypertensionEnrichmentACVRL1, BMPR2, GDF2, SMAD98.14
2Hereditary hemorrhagic telangiectasiaEnrichmentACVRL1, GDF2, SMAD46.42
3Pulmonary hypertension, primary, 1EnrichmentACVRL1, BMPR2, GDF25.52
4Craniosynostosis 7EnrichmentBMP2, SMAD65.30
5Hereditary mixed polyposis syndromeEnrichmentBMPR1A, GREM15.24
6Juvenile polyposis syndromeEnrichmentBMPR1A, SMAD44.82
7Pulmonary arterial hypertension associated with congenital heart diseaseEnrichmentBMPR2, SMAD94.82
8Brachydactyly, type a2EnrichmentBMP2, BMPR1B4.52
9Persistent mullerian duct syndrome, types i and iiEnrichmentAMH, AMHR24.52
10Persistent mullerian duct syndromeEnrichmentAMH, AMHR24.52
11Generalized juvenile polyposis/juvenile polyposis coliEnrichmentBMPR1A, SMAD44.30
12Ventricular septal defect 1EnrichmentBMP2, BMP74.24
13Familial thoracic aortic aneurysm and aortic dissectionEnrichmentSKI, SMAD43.99
14Hemochromatosis, type 1EnrichmentBMP2, BMP63.80
15Shprintzen-goldberg craniosynostosis syndromeEnrichmentSKI3.43
1620p12.3 microdeletion syndromeEnrichmentBMP23.43
17Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies 1EnrichmentBMP23.43
18Heritable thoracic aortic diseaseEnrichmentSMAD43.43
19Primary pulmonary hypertensionEnrichmentBMPR23.43
20Pulmonary hypertensionEnrichmentBMPR23.43
21Drug- or toxin-induced pulmonary arterial hypertensionEnrichmentBMPR23.43
22Myhre syndromeEnrichmentSMAD43.13
23Pulmonary venoocclusive disease 1, autosomal dominantEnrichmentBMPR23.13
24Juvenile polyposis/hereditary hemorrhagic telangiectasia syndromeEnrichmentSMAD43.13
25Fibrodysplasia ossificans progressivaEnrichmentBMPR23.13
26Pulmonary venoocclusive disease 1EnrichmentBMPR23.13
27Pulmonary venoocclusive diseaseEnrichmentBMPR23.13
28Idiopathic/heritable pulmonary arterial hypertensionEnrichmentBMPR23.13
29Heart, malformation ofEnrichmentMAPK1, SMAD63.07
30Transposition of the great arteries, dextro-loopedEnrichmentBMP22.96
31Goldberg-shprintzen syndromeEnrichmentSKI2.73
32Atrial septal defect 1EnrichmentBMP22.66
33Stapes ankylosis with broad thumbs and toesEnrichmentNOG2.64
34Tarsal-carpal coalition syndromeEnrichmentNOG2.64
35Telangiectasia, hereditary hemorrhagic, type 2EnrichmentACVRL12.64
36Polyposis syndrome, hereditary mixed, 2EnrichmentBMPR1A2.64
37Acromesomelic dysplasia 3EnrichmentBMPR1B2.64
38Brachydactyly, type b2EnrichmentNOG2.64
39Symphalangism, proximal, 1aEnrichmentNOG2.64
40Multiple synostoses syndrome 1EnrichmentNOG2.64
41Brachydactyly, type a1, dEnrichmentBMPR1B2.64
42Radioulnar synostosis, nonsyndromicEnrichmentSMAD62.64
43Tooth agenesis, selective, 9EnrichmentGREM22.64
44Ovary adenocarcinomaEnrichmentINHBA2.64
45Telangiectasia, hereditary hemorrhagic, type 5EnrichmentGDF22.64
46Pulmonary hypertension, primary, 2EnrichmentSMAD92.64
47Colorectal cancer 3EnrichmentSMAD72.64
48TelangiectasisEnrichmentACVRL12.64
49Isolated congenital megalocorneaEnrichmentCHRDL12.64
50Cardiospondylocarpofacial syndromeEnrichmentMAP3K72.61
51Lymphoproliferative syndrome, x-linked, 2EnrichmentXIAP2.61
52Frontometaphyseal dysplasia 2EnrichmentMAP3K72.61
53Alopecia-intellectual disability syndrome 1EnrichmentAHSG2.61
54Noonan syndrome 13EnrichmentMAPK12.61
55Iron overloadEnrichmentBMP62.61
56Encephalopathy, acute, infection-induced 9EnrichmentNUP2142.61
57Gallbladder cancerEnrichmentSMAD42.59
58Tooth agenesis, selective, 1EnrichmentBMPR22.48
59Heterotaxy, visceral, 4, autosomalEnrichmentACVR2B2.34
60Aortic valve disease 2EnrichmentSMAD62.34
61Proximal symphalangismEnrichmentNOG2.34
62Radioulnar synostosisEnrichmentSMAD62.34
63Juvenile polyposis of infancyEnrichmentBMPR1A2.34
64Chromosome 1p36 deletion syndromeEnrichmentSKI2.32
65Acute myeloid leukemia with t(6;9) (p23;q34.1)EnrichmentNUP2142.31
66ThrombocytopeniaEnrichmentACVRL1, SMAD42.27
67Brachydactyly, type a1EnrichmentBMPR1B2.16
68Brachydactyly, type cEnrichmentBMPR1B2.16
69Acromesomelic dysplasia 2aEnrichmentBMPR1B2.16
70Acromesomelic dysplasia 2cEnrichmentBMPR1B2.16
71MegalocorneaEnrichmentCHRDL12.16
72Acromesomelic dysplasia 2bEnrichmentBMPR1B2.16
73Arteriovenous malformations of the brainEnrichmentZFYVE162.16
74Frontometaphyseal dysplasiaEnrichmentMAP3K72.14
75Alopecia - intellectual disability syndromeEnrichmentAHSG2.14
76Hemophilia aEnrichmentACVRL12.04
77Factor viii deficiencyEnrichmentACVRL12.04
78Multiple synostoses syndromeEnrichmentNOG2.04
79Pancreatic cancerEnrichmentSMAD42.04
80Polyposis syndrome, hereditary mixed, 1EnrichmentGREM12.01
81Chromosome 22q11.2 deletion syndrome, distalEnrichmentMAPK12.01
82Lymphoproliferative syndrome 2EnrichmentXIAP2.01
83Orofacial cleftEnrichmentFST2.01
84Orofacial clefting syndromeEnrichmentFST2.01
852q23.1 microduplication syndromeEnrichmentACVR2A1.94
86Familial cerebral saccular aneurysmEnrichmentTGFBR31.94
87Congenital heart defects, multiple types, 4EnrichmentBMP71.92
88Telangiectasia, hereditary hemorrhagic, type 1EnrichmentACVRL11.87
89Gastric cancerEnrichmentSMAD41.80
90PolydactylyEnrichmentSMAD61.69
91Familial colorectal cancerEnrichmentGREM11.62
92Familial colorectal cancer type xEnrichmentBMPR1A1.60
93Specific learning disabilityEnrichmentMAPK11.58
94Aortic valve disease 1EnrichmentSMAD61.53
95Aortic aneurysm, familial thoracic 1EnrichmentSMAD61.50
96Colorectal cancerEnrichmentSMAD41.50
97Inherited cancer-predisposing syndromeEnrichmentBMPR1A, SMAD41.44
98CraniosynostosisEnrichmentSMAD61.35
99Visceral heterotaxyEnrichmentACVR2B1.31
100Tooth agenesisEnrichmentGREM21.31
101Precursor t-cell acute lymphoblastic leukemiaEnrichmentNUP2141.26
102Autoinflammatory diseaseEnrichmentXIAP1.25
103Leukemia, acute myeloidEnrichmentNUP2141.03
104Primary ovarian insufficiencyEnrichmentBMP60.87
105Ovarian cancerEnrichmentBMPR1A0.68
106MicrocephalyEnrichmentMAPK10.59

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