Matrix metalloproteinases

Pathway network for the Matrix metalloproteinases SuperPath

Sources:
  • WikiPathways
  • QIAGEN
  • Reactome

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

Disorders associated with Matrix metalloproteinases SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Metaphyseal anadysplasiaEnrichmentMMP13, MMP95.30
2Multicentric osteolysis, nodulosis, and arthropathyEnrichmentMMP14, MMP24.82
3Chromosome 1p36 deletion syndromeEnrichmentHSPG2, MMP23B3.28
4Pancreatitis, hereditaryEnrichmentPRSS1, PRSS23.12
5Cavitary optic disc anomaliesEnrichmentMMP192.64
6Winchester syndromeEnrichmentMMP142.64
7Heterotaxy, visceral, 7, autosomalEnrichmentMMP212.64
8Coronary heart disease 6EnrichmentMMP32.64
9Developmental delay with variable intellectual impairment and behavioral abnormalitiesEnrichmentTCF202.64
10PycnodysostosisEnrichmentCTSK2.61
11Prekallikrein deficiencyEnrichmentKLKB12.61
12Angioedema, hereditary, 4EnrichmentPLG2.61
13Inherited prekallikrein deficiencyEnrichmentKLKB12.61
14Alzheimer disease 18EnrichmentADAM102.58
15Reticulate acropigmentation of kitamuraEnrichmentADAM102.58
16Sorsby fundus dystrophyEnrichmentTIMP32.34
17Metaphyseal dysplasia, spahr typeEnrichmentMMP132.34
18Spondyloepimetaphyseal dysplasia, missouri typeEnrichmentMMP132.34
19Amelogenesis imperfecta, hypomaturation type, iia2EnrichmentMMP202.34
20Immunodeficiency 127EnrichmentTNF2.34
21Recessive dystrophic epidermolysis bullosaEnrichmentMMP12.34
22Preterm premature rupture of the membranesEnrichmentMMP82.34
23Metaphyseal anadysplasia 2EnrichmentMMP92.34
24Cyclic neutropeniaEnrichmentELANE2.31
25Plasminogen deficiency, type iEnrichmentPLG2.31
26Neutropenia, severe congenital, x-linkedEnrichmentELANE2.31
27Glaucoma, primary closed-angleEnrichmentCOL18A12.31
28Hereditary angioedemaEnrichmentPLG2.31
29Trypsinogen deficiencyEnrichmentPRSS12.31
30Schwartz-jampel syndrome, type 1EnrichmentHSPG22.28
31Inflammatory skin and bowel disease, neonatal, 1EnrichmentADAM172.28
32Psoriatic arthritisEnrichmentTNF2.16
33Migraine without auraEnrichmentTNF2.16
34Angioedema, hereditary, 1EnrichmentPLG2.14
35Neutropenia, severe congenital, 1, autosomal dominantEnrichmentELANE2.14
36Nail disorder, nonsyndromic congenital, 9EnrichmentCTSK2.14
37Dyssegmental dysplasia, silverman-handmaker typeEnrichmentHSPG22.10
38Ehlers-danlos syndrome, classic-like, 3EnrichmentTHBS22.10
39Neonatal inflammatory skin and bowel diseaseEnrichmentADAM172.10
40Cerebral malariaEnrichmentTNF2.04
41Knobloch syndromeEnrichmentCOL18A12.01
42Dowling-degos disease 1EnrichmentADAM101.98
43Vascular dementiaEnrichmentTNF1.94
44Vitamin d-dependent rickets, type 2aEnrichmentPRSS11.92
45Knobloch syndrome 1EnrichmentCOL18A11.92
46Autosomal dominant severe congenital neutropeniaEnrichmentELANE1.92
47Amelogenesis imperfecta type 2EnrichmentMMP201.80
48NeutropeniaEnrichmentELANE1.77
49Intervertebral disc diseaseEnrichmentTHBS21.73
50Primary bone dysplasiaEnrichmentCTSK1.62
51Pectus excavatumEnrichmentTCF201.60
52AsthmaEnrichmentTNF1.60
53OsteochondrodysplasiaEnrichmentCTSK1.58
54Alzheimer's diseaseEnrichmentTNF1.53
55CataractEnrichmentCOL18A11.47
56Hereditary chronic pancreatitisEnrichmentPRSS11.47
57Arteriovenous malformations of the brainEnrichmentTIMP31.37
58CraniosynostosisEnrichmentTCF201.35
59Attention deficit-hyperactivity disorderEnrichmentTCF201.31
60Visceral heterotaxyEnrichmentMMP211.31
61Ehlers-danlos syndromeEnrichmentTHBS21.31
62MalariaEnrichmentTNF1.29
63Autoinflammatory diseaseEnrichmentELANE1.25
64ScoliosisEnrichmentCTSK1.25
65Visceral heterotaxy 5EnrichmentMMP211.16
66Stargardt disease 1EnrichmentCOL18A11.15
67Cystic fibrosisEnrichmentPLG1.12
68Systemic lupus erythematosusEnrichmentTNF1.07
69AutismEnrichmentTCF200.82
70Autism spectrum disorderEnrichmentTCF200.65
71Complex neurodevelopmental disorderEnrichmentTCF200.61
72Retinitis pigmentosaEnrichmentCOL18A10.39
73Hereditary retinal dystrophyEnrichmentTIMP30.31
74Fundus dystrophyEnrichmentTIMP30.31

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