Leukocyte-intrinsic Hippo pathway functions

No Pathway Network information available for Leukocyte-intrinsic Hippo pathway functions

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

Disorders associated with Leukocyte-intrinsic Hippo pathway functions SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Malignant peritoneal mesotheliomaEnrichmentLATS1, LATS25.27
2Immunodysregulation, polyendocrinopathy, and enteropathy, x-linkedEnrichmentFOXP32.63
3Coloboma, ocular, with or without hearing impairment, cleft lip/palate, and/or impaired intellectual developmentEnrichmentYAP12.63
4Thrombocytopenia 3EnrichmentFYB12.63
5Uveal coloboma-cleft lip and palate-intellectual disabilityEnrichmentYAP12.63
6Immunodeficiency, common variable, 3EnrichmentCD192.63
7Congenital autosomal recessive small-platelet thrombocytopeniaEnrichmentFYB12.63
8Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndromEnrichmentRAC12.63
9Leukocyte adhesion deficiency, type iEnrichmentFERMT32.33
10Sveinsson chorioretinal atrophyEnrichmentTEAD12.33
11Multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, and hydranencephalyEnrichmentFOXP32.33
12Hyperlipoproteinemia, type iEnrichmentLPL2.33
13Leukocyte adhesion deficiency, type iiiEnrichmentFERMT32.33
14Roifman-chitayat syndromeEnrichmentKNSTRN2.33
15Lipase deficiency, combinedEnrichmentLPL2.33
16Charcot-marie-tooth disease, demyelinating, type 4dEnrichmentNDRG12.33
17Intellectual developmental disorder, autosomal dominant 48EnrichmentRAC12.33
18Retinitis pigmentosa 14EnrichmentTEAD32.33
19Familial lipoprotein lipase deficiencyEnrichmentLPL2.33
20Charcot-marie-tooth disease type 4dEnrichmentNDRG12.33
21Common variable immunodeficiency phenotype due to cd19/cd81 deficiencyEnrichmentCD192.33
22Barth syndromeEnrichmentTAFAZZIN2.15
23Myeloma, multipleEnrichmentLATS1, YAP12.12
24Malignant epithelioid hemangioendotheliomaEnrichmentYAP12.03
25Coronary artery anomalyEnrichmentLPL2.03
26Hyperlipidemia, familial combined, 3EnrichmentLPL1.93
27Rhabdomyosarcoma 2EnrichmentFOXO11.93
28Cholangitis, primary sclerosingEnrichmentMST11.93
29Type 1 diabetes mellitusEnrichmentFOXP31.85
30Neurodevelopmental disorder with dysmorphic facies and distal limb anomaliesEnrichmentRAC11.68
31Hydrops fetalisEnrichmentFOXP31.68
32Microphthalmia/coloboma 12EnrichmentYAP11.52
33Coloboma of maculaEnrichmentYAP11.46
34Charcot-marie-tooth disease type 4EnrichmentNDRG11.38
35Diffuse large b-cell lymphomaEnrichmentFOXO11.36
36Cardiomyopathy, dilated, 1aEnrichmentLPL1.31
37Centronuclear myopathyEnrichmentFOXP31.31
38Left ventricular noncompactionEnrichmentTAFAZZIN1.10
39Charcot-marie-tooth diseaseEnrichmentNDRG11.03
40Familial isolated dilated cardiomyopathyEnrichmentTAFAZZIN0.93
41Dilated cardiomyopathyEnrichmentTAFAZZIN0.76
42Leber plus diseaseEnrichmentTEAD30.70
43Hereditary retinal dystrophyEnrichmentTEAD30.30
44Fundus dystrophyEnrichmentTEAD30.30

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