Hippo-YAP signaling

No Pathway Network information available for Hippo-YAP signaling

Pathways in the Hippo-YAP signaling SuperPath

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

Disorders associated with Hippo-YAP signaling SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Schwannomatosis, vestibularEnrichmentNF22.90
2Intellectual developmental disorder, autosomal recessive 54EnrichmentTNIK2.90
3Acoustic neuromaEnrichmentNF22.90
4Sveinsson chorioretinal atrophyEnrichmentTEAD12.60
5Grange syndromeEnrichmentYY1AP12.60
6Schwannomatosis 1EnrichmentNF22.60
7Charcot-marie-tooth disease, demyelinating, type 4dEnrichmentNDRG12.60
8Retinitis pigmentosa 14EnrichmentTEAD32.60
9Charcot-marie-tooth disease type 4dEnrichmentNDRG12.60
10Malignant peritoneal mesotheliomaEnrichmentLATS12.60
11Barth syndromeEnrichmentTAFAZZIN2.43
12Anus, imperforateEnrichmentMAP4K42.43
13Cellular ependymomaEnrichmentNF22.43
14Tanycytic ependymomaEnrichmentNF22.43
15Papillary ependymomaEnrichmentNF22.43
16Spindle cell sarcomaEnrichmentNF22.43
17Clear cell ependymomaEnrichmentNF22.43
18Ciliary dyskinesia, primary, 22EnrichmentRASSF12.30
19Full schwannomatosisEnrichmentNF22.30
20Benign ependymomaEnrichmentNF22.30
21Myasthenic syndrome, congenital, 4a, slow-channelEnrichmentMINK12.20
22Cholangitis, primary sclerosingEnrichmentMST12.20
23Myasthenic syndrome, congenital, 4b, fast-channelEnrichmentMINK12.20
24Multiple endocrine neoplasia, type iEnrichmentMAP4K22.06
25Myasthenic syndrome, congenital, 1a, slow-channelEnrichmentMINK12.06
26Renal hypodysplasia/aplasia 1EnrichmentMAP4K42.00
27Inherited cancer-predisposing syndromeEnrichmentMAP4K2, NF21.93
28Myasthenic syndrome, congenital, 4c, associated with acetylcholine receptor deficiencyEnrichmentMINK11.90
29Meningioma, familialEnrichmentNF21.86
30MeningiomaEnrichmentNF21.83
31Congenital myasthenic syndromeEnrichmentMINK11.76
32Charcot-marie-tooth disease type 4EnrichmentNDRG11.65
33Arteriovenous malformations of the brainEnrichmentMAP4K41.63
34Left ventricular noncompactionEnrichmentTAFAZZIN1.37
35Charcot-marie-tooth diseaseEnrichmentNDRG11.30
36Familial isolated dilated cardiomyopathyEnrichmentTAFAZZIN1.19
37Myeloma, multipleEnrichmentLATS11.17
38Autosomal recessive non-syndromic intellectual disabilityEnrichmentTNIK1.15
39Dilated cardiomyopathyEnrichmentTAFAZZIN1.02
40Leber plus diseaseEnrichmentTEAD30.95
41Hereditary retinal dystrophyEnrichmentTEAD30.51
42Fundus dystrophyEnrichmentTEAD30.51

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