Intra-Golgi traffic

No Pathway Network information available for Intra-Golgi traffic

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

Disorders associated with Intra-Golgi traffic SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Achondrogenesis, type iaEnrichmentTRIP112.49
2Congenital disorder of glycosylation, type iilEnrichmentCOG62.49
3Odontochondrodysplasia 1EnrichmentTRIP112.49
4Congenital disorder of glycosylation, type iijEnrichmentCOG42.49
5Congenital disorder of glycosylation, type iiqEnrichmentCOG22.49
6Developmental and epileptic encephalopathy 107EnrichmentNAPB2.49
7Saul-wilson syndromeEnrichmentCOG42.49
8Congenital disorder of glycosylation, type iiaaEnrichmentSTX52.49
9Shaheen syndromeEnrichmentCOG62.49
10Neutropenia, severe congenital, 5, autosomal recessiveEnrichmentVPS452.49
11Cog4-congenital disorder of glycosylationEnrichmentCOG42.49
12Congenital disorder of glycosylation, type iibbEnrichmentCOG32.49
13Severe congenital neutropenia 5EnrichmentVPS452.49
14Cog6-congenital disorder of glycosylationEnrichmentCOG62.49
15Hypohidrosis-enamel hypoplasia-palmoplantar keratoderma-intellectual disability syndromeEnrichmentCOG62.49
16Amyotrophy, hereditary neuralgicEnrichmentNAPB2.19
17Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndromeEnrichmentSNAP292.19
18Congenital disorder of glycosylation, type iihEnrichmentCOG82.19
19Catifa syndromeEnrichmentRIC12.19
20Periventricular nodular heterotopia 8EnrichmentARF12.19
21Neurodevelopmental disorder with developmental delay and with or without motor or speech delayEnrichmentCUX12.19
22Smith-mccort dysplasiaEnrichmentRAB33B2.19
23Developmental and epileptic encephalopathy 96EnrichmentNSF2.19
24Smith-mccort dysplasia 2EnrichmentRAB33B2.19
25Cog8-congenital disorder of glycosylationEnrichmentCOG82.19
26Congenital disorder of glycosylation, type iigEnrichmentCOG12.01
27Leukodystrophy, hypomyelinating, 2EnrichmentSNAP292.01
28Epilepsy, progressive myoclonic, 6EnrichmentGOSR22.01
29Muscular dystrophy, congenital, with or without seizuresEnrichmentGOSR22.01
30Cog7-congenital disorder of glycosylationEnrichmentCOG72.01
31Pseudohypoparathyroidism, type ibEnrichmentSTX161.89
32Congenital disorder of glycosylation, type iiiEnrichmentCOG51.89
33Cog5-congenital disorder of glycosylationEnrichmentCOG51.89
34Immunodeficiency 47EnrichmentCOG71.59
35Severe congenital neutropeniaEnrichmentVPS451.59
36Progressive myoclonus epilepsyEnrichmentGOSR21.50
37Myoclonic epilepsy of unverricht and lundborgEnrichmentGOSR21.35
38Periventricular nodular heterotopiaEnrichmentARF11.35
39Cleft lip/palateEnrichmentRIC11.35
40Differentiated thyroid carcinomaEnrichmentGOLGA51.05
41Connective tissue diseaseEnrichmentTRIP111.01
42Autosomal dominant non-syndromic intellectual disabilityEnrichmentCUX10.82
43Deafness, autosomal recessiveEnrichmentGOSR20.73
44Autosomal recessive nonsyndromic deafnessEnrichmentGOSR20.73
45Rare autosomal recessive non-syndromic sensorineural deafness type dfnbEnrichmentGOSR20.60

Loading...
Loading...
Loading...