RHOH GTPase cycle

No Pathway Network information available for RHOH GTPase cycle

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

Disorders associated with RHOH GTPase cycle SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Mosaic variegated aneuploidy syndrome 1EnrichmentBUB1B-PAK6, PAK64.12
2Mosaic variegated aneuploidy syndromeEnrichmentBUB1B-PAK6, PAK63.67
3Combined immunodeficiencyEnrichmentTFRC, ZAP703.38
4Combined t cell and b cell immunodeficiencyEnrichmentTFRC, ZAP703.38
5Combined t and b cell immunodeficiencyEnrichmentTFRC, ZAP703.38
6Arrhythmogenic right ventricular dysplasia, familial, 12EnrichmentJUP2.55
7Lipodystrophy, congenital generalized, type 3EnrichmentCAV12.55
8Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1EnrichmentVCP2.55
9Hypogonadotropic hypogonadism 14 with or without anosmiaEnrichmentWDR112.55
10Nephrotic syndrome, type 8EnrichmentARHGDIA2.55
11Pulmonary hypertension, primary, 3EnrichmentCAV12.55
12Naxos diseaseEnrichmentJUP2.55
13Intellectual developmental disorder, autosomal recessive 78EnrichmentWDR112.55
14Maple syrup urine disease, type iiEnrichmentDBT2.55
15Knobloch syndrome 2EnrichmentPAK22.55
16Charcot-marie-tooth disease, axonal, type 2bEnrichmentRAB7A2.55
17Immunodeficiency 48EnrichmentZAP702.55
18Intellectual developmental disorder with macrocephaly, seizures, and speech delayEnrichmentPAK12.55
19Charcot-marie-tooth disease type 2bEnrichmentRAB7A2.55
20Lipodystrophy, familial partial, type 7EnrichmentCAV12.55
21Immunodeficiency 46EnrichmentTFRC2.55
22Frontotemporal dementia and/or amyotrophic lateral sclerosis 6EnrichmentVCP2.55
23Autoimmune disease, multisystem, infantile-onset, 2EnrichmentZAP702.55
24Immunodeficiency 22EnrichmentLCK2.55
25Neurodevelopmental disorder with hypotonia, neonatal respiratory insufficiency, and thermodysregulationEnrichmentRALGAPA12.55
26Multisystem proteinopathyEnrichmentVCP2.55
27Immunodeficiency 129EnrichmentRHOH2.55
28Adult-onset distal myopathy due to vcp mutationEnrichmentVCP2.55
29T-cell immunodeficiency with epidermodysplasia verruciformisEnrichmentRHOH2.55
30Zap70-related severe combined immunodeficiencyEnrichmentZAP702.55
31Severe combined immunodeficiencyEnrichmentLCK, ZAP702.42
32Amyotrophic lateral sclerosis 6 with or without frontotemporal dementiaEnrichmentVCP2.25
33Disorders of intracellular cobalamin metabolismEnrichmentMTR2.25
34Spastic paraplegia-paget disease of bone syndromeEnrichmentVCP2.25
35Maple syrup urine disease, type iaEnrichmentDBT2.08
36Homocystinuria-megaloblastic anemia, cblg typeEnrichmentMTR2.08
37Epidermolysis bullosa, lethal acantholyticEnrichmentJUP2.08
38Estrogen resistanceEnrichmentTMEM592.08
39Inclusion body myopathy with paget disease of bone and frontotemporal dementiaEnrichmentVCP2.08
40HomocystinuriaEnrichmentMTR2.08
41Intermittent maple syrup urine diseaseEnrichmentDBT2.08
42Classic maple syrup urine diseaseEnrichmentDBT2.08
43Sacral defect with anterior meningoceleEnrichmentVANGL11.95
44Neural tube defects, folate-sensitiveEnrichmentMTR1.95
45Knobloch syndromeEnrichmentPAK21.95
46Intermediate maple syrup urine diseaseEnrichmentDBT1.95
47Dementia, lewy bodyEnrichmentVCP1.86
48Knobloch syndrome 1EnrichmentPAK21.86
49Charcot-marie-tooth disease, axonal, type 2eEnrichmentVCP1.86
50Diffuse cutaneous systemic sclerosisEnrichmentCAV11.86
51Limited sclerodermaEnrichmentCAV11.78
52Progressive non-fluent aphasiaEnrichmentVCP1.60
53Behavioral variant of frontotemporal dementiaEnrichmentVCP1.60
54Frontotemporal dementia and/or amyotrophic lateral sclerosis 1EnrichmentVCP1.56
55Heritable pulmonary arterial hypertensionEnrichmentCAV11.52
56Inherited isolated arrhythmogenic ventricular dysplasia, biventricular variantEnrichmentJUP1.48
57Inherited isolated arrhythmogenic cardiomyopathy, dominant-left variantEnrichmentJUP1.48
58Neural tube defectsEnrichmentVANGL11.45
59Alzheimer's diseaseEnrichmentVCP1.45
60Inherited isolated arrhythmogenic cardiomyopathy, dominant-right variantEnrichmentJUP1.41
61Pituitary stalk interruption syndromeEnrichmentWDR111.41
62Wolff-parkinson-white syndromeEnrichmentJUP1.36
63Arrhythmogenic right ventricular cardiomyopathyEnrichmentJUP1.36
64Alzheimer disease, familial, 1EnrichmentVCP1.33
65Normosmic congenital hypogonadotropic hypogonadismEnrichmentWDR111.31
66Neuropathy, hereditary motor and sensory, okinawa typeEnrichmentVCP1.28
67Kallmann syndromeEnrichmentWDR111.20
68Genetic steroid-resistant nephrotic syndromeEnrichmentARHGDIA1.04
69EpilepsyEnrichmentMTR0.97
70West syndromeEnrichmentRALGAPA10.93
71Frontotemporal dementia and/or amyotrophic lateral sclerosis 7EnrichmentVCP0.82
72Dilated cardiomyopathyEnrichmentJUP0.70
73MicrocephalyEnrichmentWDR110.53

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