Cerebral dysgenesis–neuropathy–ichthyosis–keratoderma syndrome
Cerebral dysgenesis–neuropathy–ichthyosis–keratoderma syndrome |
---|
Classification and external resources |
---|
OMIM |
609528 |
---|
Cerebral dysgenesis–neuropathy–ichthyosis–keratoderma syndrome (also known as "CEDNIK syndrome") is a cutaneous condition caused by mutation in the SNAP29 gene.[1]
See also
References
- ↑ Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. ISBN 1-4160-2999-0.
|
---|
| Vesicle formation | |
---|
| Rab | |
---|
| Cytoskeleton | |
---|
| Vesicle fusion | |
---|
| See also vesicular transport proteins
Index of cells |
---|
| Description |
- Structure
- Organelles
- peroxisome
- cytoskeleton
- centrosome
- epithelia
- cilia
- mitochondria
- Membranes
- Membrane transport
- ion channels
- vesicular transport
- solute carrier
- ABC transporters
- ATPase
- oxidoreduction-driven
|
---|
| Disease |
- Structural
- peroxisome
- cytoskeleton
- cilia
- mitochondria
- nucleus
- scleroprotein
- Membrane
- channelopathy
- solute carrier
- ATPase
- ABC transporters
- other
- extracellular ligands
- cell surface receptors
- intracellular signalling
- Vesicular transport
- Pore-forming toxins
|
---|
|
|