Arf1 pathway

No Pathway Network information available for Arf1 pathway

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

Disorders associated with Arf1 pathway SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Intellectual developmental disorder, autosomal dominant 60, with seizuresEnrichmentAP2M1, PIP5K1A5.39
2Developmental delay, impaired speech, and behavioral abnormalities, with or without seizuresEnrichmentARFGEF12.69
3Okt4 epitope deficiencyEnrichmentCD42.69
4Charcot-marie-tooth disease, axonal, type 2ggEnrichmentGBF12.69
5Autoinflammation and autoimmunity, systemic, with immune dysregulationEnrichmentCOPA2.69
6Immunodeficiency 79EnrichmentCD42.69
7Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndromEnrichmentRAC12.69
8Cataract 11, multiple typesEnrichmentGBF12.38
9Anterior segment dysgenesis 1EnrichmentGBF12.38
10Intellectual developmental disorder, autosomal dominant 48EnrichmentRAC12.38
11Periventricular nodular heterotopia 8EnrichmentARF12.38
12Nephrotic syndrome, type 17EnrichmentGGA32.38
13Joubert syndrome 21EnrichmentARFGEF12.38
14Epilepsy, progressive myoclonic, 6EnrichmentGOSR22.21
15Muscular dystrophy, congenital, with or without seizuresEnrichmentGOSR22.21
16Myoclonic-atonic epilepsyEnrichmentAP2M11.73
17Neurodevelopmental disorder with dysmorphic facies and distal limb anomaliesEnrichmentRAC11.73
18Progressive myoclonus epilepsyEnrichmentGOSR21.69
19Myoclonic epilepsy of unverricht and lundborgEnrichmentGOSR21.54
20Periventricular nodular heterotopiaEnrichmentARF11.54
21Deafness, autosomal recessiveEnrichmentGOSR20.91
22Autosomal recessive nonsyndromic deafnessEnrichmentGOSR20.91
23Rare autosomal recessive non-syndromic sensorineural deafness type dfnbEnrichmentGOSR20.77

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