Oligomerization of connexins into connexons

No Pathway Network information available for Oligomerization of connexins into connexons

Pathways in the Oligomerization of connexins into connexons SuperPath

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

Disorders associated with Oligomerization of connexins into connexons SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Rare autosomal recessive non-syndromic sensorineural deafness type dfnbEnrichmentGJA1, GJB23.90
2Palmoplantar keratoderma and congenital alopecia 1EnrichmentGJA13.66
3Bart-pumphrey syndromeEnrichmentGJB23.66
4Vohwinkel syndromeEnrichmentGJB23.66
5Hypoplastic left heart syndrome 1EnrichmentGJA13.66
6Deafness, autosomal dominant 3aEnrichmentGJB23.66
7Keratitis-ichthyosis-deafness syndrome, autosomal dominantEnrichmentGJB23.66
8Oculodentodigital dysplasiaEnrichmentGJA13.66
9Craniometaphyseal dysplasia, autosomal recessiveEnrichmentGJA13.66
10Ichthyosis, hystrix-like, with deafnessEnrichmentGJB23.66
11Oculodentodigital dysplasia, autosomal recessiveEnrichmentGJA13.66
12Erythrokeratodermia variabilis et progressiva 3EnrichmentGJA13.66
13Porokeratotic eccrine ostial and dermal duct nevusEnrichmentGJB23.66
14Autosomal dominant nonsyndromic hearing loss 3aEnrichmentGJB23.66
15Spinocerebellar ataxia, x-linked 1EnrichmentGJB13.35
16Hallermann-streiff syndromeEnrichmentGJA13.35
17Syndactyly, type iiiEnrichmentGJA13.35
18Syndactyly, type vEnrichmentGJA13.35
19Deafness, autosomal recessive 104EnrichmentGJB23.35
20Craniometaphyseal dysplasiaEnrichmentGJA13.35
21Deafness, autosomal recessive 1bEnrichmentGJB23.35
22Keratitis ichthyosis and deafness syndromeEnrichmentGJB23.35
23Hereditary palmoplantar keratodermaEnrichmentGJB23.35
24Keratoderma, palmoplantar, with deafnessEnrichmentGJB23.18
25Ifap syndrome 1, with or without bresheck syndromeEnrichmentGJB23.18
26Charcot-marie-tooth disease, x-linked dominant, 1EnrichmentGJB13.18
27Deafness, x-linked 2EnrichmentGJB23.18
28X-linked mixed hearing loss with perilymphatic gusherEnrichmentGJB23.18
29Deafness, autosomal recessive 1aEnrichmentGJB23.05
30Gjb2-related autosomal recessive nonsyndromic hearing lossEnrichmentGJB23.05
31Hypertrophic neuropathy of dejerine-sottasEnrichmentGJB12.96
32Cleft upper lipEnrichmentGJA12.96
33Sensory peripheral neuropathyEnrichmentGJB12.96
34Deafness, autosomal recessive 12EnrichmentGJB22.88
35Pain disorderEnrichmentGJB12.88
36Erythrokeratodermia variabilis et progressiva 1EnrichmentGJA12.75
37Hypoplastic left heart syndromeEnrichmentGJA12.75
38Noonan syndrome 1EnrichmentGJB22.29
39Ear malformationEnrichmentGJB22.28
40Peripheral nervous system diseaseEnrichmentGJB12.15
41NeuropathyEnrichmentGJB12.15
42Non-syndromic genetic deafnessEnrichmentGJB22.10
43Charcot-marie-tooth diseaseEnrichmentGJB12.04
44Nonsyndromic hearing lossEnrichmentGJB22.03
45Sensorineural hearing lossEnrichmentGJB21.98
46Rare autosomal dominant non-syndromic sensorineural deafness type dfnaEnrichmentGJB21.94
47Deafness, autosomal recessiveEnrichmentGJB21.86
48Autosomal recessive nonsyndromic deafnessEnrichmentGJB21.85
49Rare genetic deafnessEnrichmentGJB21.76
50Autism spectrum disorderEnrichmentGJB21.62

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