ADTB3AAmyotrophic lateral sclerosis slow progressing ALS8Amyotrophic lateral sclerosisARC syndromeARL6Bardet Biedl syndromebeta Actinbeta3 spectrinCadherin15Cadherin23CEDNIK syndromeCell secretion (Intracellular transport)Charcot Marie Tooth disease type 2aCharcot Marie Tooth disease type 2bChediak Higashi syndromeChoroideremiaCOG7Congenital disorder of glycosylation type IIeCranio lenticulo sutural dysplasia
Deafness (Inherited)Developmental malformations deafness dystonia OMIM_607371DTNBP1DysferlinEar (Development)Elajalde syndrome Griscelli syndrome IIFactor V (Coagulation)Factor VIII (Coagulation)Familial hemophagoctic lymphohistiocytosisGriscelli s syndrome IIIGriscelli s syndrome2HarmoninHereditary spastic paraplegia SPG10Hereditary spastic paraplegia SPG4Hermansky Pudlak syndromeHPS1HPS3HPS4HPS5
HPS6KIF1BKIF5ALimb girdle muscular dystrophy type 2BLMAN1 ERGIC53Lowe s syndromeLYST CHS1Martsolf syndromeMCFD2Miyoshi s myopathyMLPHMyosin Ia Myo1aMyosin Va Myo5aMyosin VIIaMyosin XVa Myo15aOCRL1OMIM_300104RAB27ARAB3GAP
RAB7RABGDIAREP1SansSEC23ASNAP29SPG20 SpartinSPG4 SpastinSpinal muscular atrophy late onsetSpinocerebellar ataxia5Syntaxin11Troyer syndrome SPG20UNC13D Munc13 4 HPLH3Usher s syndromeUsher syndrome type IbVAPBVPS33BWarburg Micro syndrome
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