ADTB3AAmyotrophic lateral sclerosis slow progressing ALS8Amyotrophic lateral sclerosisAP3B1ARC syndromeARL6Bardet Biedl syndromebeta Actinbeta3 spectrinBIRC4CEDNIK syndromeCell secretion (Intracellular transport)Charcot Marie Tooth disease type 2aCharcot Marie Tooth disease type 2bChediak Higashi syndromeChoroideremiaCOG7Congenital disorder of glycosylation type IIeCranio lenticulo sutural dysplasiaDeafness (Inherited)
Developmental malformations deafness dystonia OMIM_607371DTNBP1DysferlinElajalde syndrome Griscelli syndrome IIFactor V (Coagulation)Factor VIII (Coagulation)Familial hemophagoctic lymphohistiocytosisGriscelli s syndrome IIIGriscelli s syndrome2Hemophagocytic lymphohistiocytosisHereditary spastic paraplegia SPG10Hereditary spastic paraplegia SPG4Hermansky Pudlak syndromeHPS1HPS3HPS4HPS5HPS6KIF1BKIF5A
Limb girdle muscular dystrophy type 2BLMAN1 ERGIC53Lowe s syndromeLYST CHS1Martsolf syndromeMCFD2Miyoshi s myopathyMLPHMyosin Ia Myo1aMyosin Va Myo5aMyosin VIMyosin VIIaMyosin XVa Myo15aOCRL1OMIM_300104PRF1RAB27ARAB3GAPRAB7RABGDIA
REP1SEC23ASH2D1ASNAP29SPG20 SpartinSPG4 SpastinSpinal muscular atrophy late onsetSpinocerebellar ataxia5STX11STXBP2Syntaxin11Troyer syndrome SPG20UNC13D Munc13 4 HPLH3Usher syndrome type IbVAPBVPS33BWarburg Micro syndrome
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