RAB geranylgeranylation

No Pathway Network information available for RAB geranylgeranylation

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

Disorders associated with RAB geranylgeranylation SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Waisman syndromeEnrichmentRAB39B2.32
2Griscelli syndrome, type 2EnrichmentRAB27A2.32
3Parkinson disease 26, autosomal dominantEnrichmentRAB322.32
4Charcot-marie-tooth disease, axonal, type 2bEnrichmentRAB7A2.32
5Charcot-marie-tooth disease type 2bEnrichmentRAB7A2.32
6Intellectual developmental disorder, x-linked 72EnrichmentRAB39B2.32
7Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matterEnrichmentRAB11B2.32
8Warburg micro syndrome 3EnrichmentRAB182.32
9Griscelli syndromeEnrichmentRAB27A2.32
10Orofaciodigital syndrome xxEnrichmentRAB342.32
11Auditory neuropathyEnrichmentRAB33A, RAB9B2.17
12Spondyloepimetaphyseal dysplasia, x-linked, with hypomyelinating leukodystrophyEnrichmentRAB33A2.02
13Charcot-marie-tooth disease, x-linked recessive, 4, with or without cerebellar ataxiaEnrichmentRAB33A2.02
14Combined oxidative phosphorylation deficiency 6EnrichmentRAB33A2.02
15Carpenter syndrome 1EnrichmentRAB232.02
16Smith-mccort dysplasiaEnrichmentRAB33B2.02
17Smith-mccort dysplasia 2EnrichmentRAB33B2.02
18Charcot-marie-tooth disease x-linked recessive 4EnrichmentRAB33A2.02
19Pelizaeus-merzbacher diseaseEnrichmentRAB9B1.84
20Spastic paraplegia 2, x-linkedEnrichmentRAB9B1.84
21Deafness, x-linked 5, with peripheral neuropathyEnrichmentRAB33A1.84
22X-linked deafness 5EnrichmentRAB33A1.84
23Combined oxidative phosphorylation deficiencyEnrichmentRAB33A1.84
24Pelizeaus-merzbacher spectrum disorderEnrichmentRAB9B1.84
25Warburg micro syndrome 1EnrichmentRAB181.72
26ChoroideremiaEnrichmentCHM1.72
27Night blindnessEnrichmentCHM1.62
28Isolated congenital microcephalyEnrichmentRAB11A1.13
29LeukodystrophyEnrichmentRAB33A1.04
30Multisystem inflammatory syndrome in childrenEnrichmentRAB27A1.00
31Autoinflammatory diseaseEnrichmentRAB27A0.96
32Asphyxiating thoracic dystrophyEnrichmentRAB340.90
33Short-rib thoracic dysplasia 1 with or without polydactylyEnrichmentRAB340.83
34Eye diseaseEnrichmentCHM0.81
35Non-syndromic x-linked intellectual disabilityEnrichmentRAB39B0.80
36Hereditary spastic paraplegiaEnrichmentRAB9B0.74
37Sensorineural hearing lossEnrichmentRAB33A0.69
38Autosomal dominant non-syndromic intellectual disabilityEnrichmentRAB11A0.67
39Retinitis pigmentosaEnrichmentCHM0.19
40Hereditary retinal dystrophyEnrichmentCHM0.12
41Fundus dystrophyEnrichmentCHM0.12

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