PTF1A related regulatory pathway

No Pathway Network information available for PTF1A related regulatory pathway

Pathways in the PTF1A related regulatory pathway SuperPath

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

Disorders associated with PTF1A related regulatory pathway SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Pancreas, dorsal, agenesis ofEnrichmentPDX1, PTF1A6.22
2Type 2 diabetes mellitusEnrichmentPDX1, RBPJ, RBPJL5.35
3Adams-oliver syndromeEnrichmentNOTCH1, RBPJ4.90
4Maturity-onset diabetes of the youngEnrichmentPDX1, PTF1A3.95
5Pancreatic agenesis 1EnrichmentPDX13.09
6Maturity-onset diabetes of the young, type 4EnrichmentPDX13.09
7Pancreatic and cerebellar agenesisEnrichmentPTF1A3.09
8Aplasia of lacrimal and salivary glandsEnrichmentFGF103.09
9Lacrimoauriculodentodigital syndrome 3EnrichmentFGF103.09
10Adenoid ameloblastomaEnrichmentCTNNB13.09
11Interstitial lung disease specific to childhoodEnrichmentFGF103.09
12Microcystic stromal tumorEnrichmentCTNNB13.09
13Osteopathia striata with cranial sclerosisEnrichmentCTNNB12.79
14Pulmonary hypoplasia, primaryEnrichmentFGF102.79
15Kallikrein, decreased urinary activity ofEnrichmentPTF1A2.79
16Adams-oliver syndrome 5EnrichmentNOTCH12.79
17Adams-oliver syndrome 3EnrichmentRBPJ2.79
18Childhood hepatocellular carcinomaEnrichmentCTNNB12.79
19Pancreatic agenesis 2EnrichmentPTF1A2.79
20Juvenile nasopharyngeal angiofibromaEnrichmentCTNNB12.79
21TeratomaEnrichmentCTNNB12.79
22Desmoid disease, hereditaryEnrichmentCTNNB12.61
23Lacrimoauriculodentodigital syndrome 1EnrichmentFGF102.61
24Neurodevelopmental disorder with spastic diplegia and visual defectsEnrichmentCTNNB12.61
25Anus, imperforateEnrichmentCTNNB12.61
26Exudative vitreoretinopathy 7EnrichmentCTNNB12.61
27Desmoid tumorEnrichmentCTNNB12.61
28KeratoacanthomaEnrichmentNOTCH12.61
29PilomatrixomaEnrichmentCTNNB12.49
30Alazami syndromeEnrichmentCTNNB12.49
31CraniopharyngiomaEnrichmentCTNNB12.49
32Exudative vitreoretinopathy 1EnrichmentCTNNB12.39
33Weyers acrofacial dysostosisEnrichmentCTNNB12.31
34Adrenocortical carcinomaEnrichmentCTNNB12.31
35Gallbladder cancerEnrichmentCTNNB12.25
36Exudative vitreoretinopathyEnrichmentCTNNB12.19
37Permanent neonatal diabetes mellitusEnrichmentPDX12.19
38Hypoplastic left heart syndromeEnrichmentNOTCH12.19
39Orofacial cleft 1EnrichmentFGF102.14
40Adult hepatocellular carcinomaEnrichmentCTNNB12.14
41Aortic valve disease 1EnrichmentNOTCH11.98
42MedulloblastomaEnrichmentCTNNB11.95
43Aortic aneurysm, familial thoracic 1EnrichmentNOTCH11.95
44Lung cancer susceptibility 3EnrichmentFGF101.95
45Polycystic liver diseaseEnrichmentCTNNB11.86
46Autosomal dominant polycystic liver diseaseEnrichmentCTNNB11.86
47HepatoblastomaEnrichmentCTNNB11.77
48Hepatocellular carcinomaEnrichmentCTNNB11.75
49Tetralogy of fallotEnrichmentNOTCH11.68
50Bladder cancerEnrichmentCTNNB11.63
51Connective tissue diseaseEnrichmentNOTCH11.59
52Familial thoracic aortic aneurysm and aortic dissectionEnrichmentNOTCH11.45
53Colorectal cancerEnrichmentCTNNB11.17
54Ovarian cancerEnrichmentCTNNB11.10
55Congenital nervous system abnormalityEnrichmentCTNNB11.08
56Nervous system diseaseEnrichmentCTNNB11.08
57MicrocephalyEnrichmentCTNNB11.02

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