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- COMPLEX MOLECULE AND ORGANELLE METABOLISM
- 19 Disorders of organelle biogenesis, dynamics and interactions
- 19.6 Disorders of vesicular trafficking
- 19.6.4 Other disorders of vesicular trafficking
- STX5-CDG
- CAMLG-CDG
- GET3 deficiency
- GET4 deficiency
- Jagunal 1 deficiency
- COPA deficiency
- COPB2 deficiency
- Archain 1 deficiency
- Craniolenticulosutural dysplasia
- Congenital dyserythropoietic anemia type 2
- TRIP11-CDG
- ATP9A deficiency
- GOSR2-CDG
- VPS4A deficiency
- VPS16 deficiency
- VPS41
- VPS45 deficiency
- VPS51 deficiency
- VPS53 deficiency
- Syndetin deficiency
- Arthrogryposis-renal dysfunction-cholestasis syndrome type 2
- YIF1B deficiency
- TANGO2 deficiency
- NBAS deficiency
- RINT1 deficiency
- SCYL1 deficiency
- SCYL2 deficiency
- SCYL1-binding protein deficiency
- Familial hemophagocytic lymphohistiocytosis
- Familial hemophagocytic lymphohistiocytosis type 3
- Familial hemophagocytic lymphohistiocytosis type 4
- Familial hemophagocytic lymphohistiocytosis type 5
- Golgin A2 deficiency
- Syntaxin 16 deficiency
- ARFGEF2 deficiency
- p34 deficiency
- Rubicon deficiency
- Grey platelet syndrome
- Combined factor V and factor VIII deficienc
- Combined factor V and factor VIII deficiency type 1
- Combined factor V and factor VIII deficiency type 2
- Dymeclin deficiency
- Carpenter syndrome
- Warburg micro syndrome
- Martsolf syndrome
- RAB18 deficiency
- RAB3GAP1 deficiency
- RAB3GAP2 deficiency
- RAB5 deficiency
- RAB33B deficiency
- 19.6.4 Other disorders of vesicular trafficking
- 19.6 Disorders of vesicular trafficking
- 19 Disorders of organelle biogenesis, dynamics and interactions
- COMPLEX MOLECULE AND ORGANELLE METABOLISM
- Genes
- Gene products
- Pathways
- Multimers
- More information
- Home
- Diseases
- COMPLEX MOLECULE AND ORGANELLE METABOLISM
- 19 Disorders of organelle biogenesis, dynamics and interactions
- 19.6 Disorders of vesicular trafficking
- 19.6.4 Other disorders of vesicular trafficking
- STX5-CDG
- CAMLG-CDG
- GET3 deficiency
- GET4 deficiency
- Jagunal 1 deficiency
- COPA deficiency
- COPB2 deficiency
- Archain 1 deficiency
- Craniolenticulosutural dysplasia
- Congenital dyserythropoietic anemia type 2
- TRIP11-CDG
- ATP9A deficiency
- GOSR2-CDG
- VPS4A deficiency
- VPS16 deficiency
- VPS41
- VPS45 deficiency
- VPS51 deficiency
- VPS53 deficiency
- Syndetin deficiency
- Arthrogryposis-renal dysfunction-cholestasis syndrome type 2
- YIF1B deficiency
- TANGO2 deficiency
- NBAS deficiency
- RINT1 deficiency
- SCYL1 deficiency
- SCYL2 deficiency
- SCYL1-binding protein deficiency
- Familial hemophagocytic lymphohistiocytosis
- Familial hemophagocytic lymphohistiocytosis type 3
- Familial hemophagocytic lymphohistiocytosis type 4
- Familial hemophagocytic lymphohistiocytosis type 5
- Golgin A2 deficiency
- Syntaxin 16 deficiency
- ARFGEF2 deficiency
- p34 deficiency
- Rubicon deficiency
- Grey platelet syndrome
- Combined factor V and factor VIII deficienc
- Combined factor V and factor VIII deficiency type 1
- Combined factor V and factor VIII deficiency type 2
- Dymeclin deficiency
- Carpenter syndrome
- Warburg micro syndrome
- Martsolf syndrome
- RAB18 deficiency
- RAB3GAP1 deficiency
- RAB3GAP2 deficiency
- RAB5 deficiency
- RAB33B deficiency
- 19.6.4 Other disorders of vesicular trafficking
- 19.6 Disorders of vesicular trafficking
- 19 Disorders of organelle biogenesis, dynamics and interactions
- COMPLEX MOLECULE AND ORGANELLE METABOLISM
- Genes
- Gene products
- Pathways
- Multimers
- More information