Ichthyosis prematurity syndrome

Ichthyosis prematurity syndrome
Classification and external resources
OMIM	608649

Ichthyosis prematurity syndrome is a cutaneous condition which has a known genetic abnormality associated with it.^[1]

It is associated with SLC27A4.

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.

Genetic disorder, membrane: Solute carrier disorders

1-10

SLC1A3
- Episodic ataxia 6
SLC2A1
- De Vivo disease
SLC2A5
- Fructose malabsorption
SLC2A10
- Arterial tortuosity syndrome
SLC3A1
- Cystinuria
SLC4A1
- Hereditary spherocytosis 4/Hereditary elliptocytosis 4
SLC4A11
- Congenital endothelial dystrophy type 2
- Fuchs' dystrophy 4
SLC5A1
- Glucose-galactose malabsorption
SLC5A2
- Renal glycosuria
SLC5A5
- Thyroid dyshormonogenesis type 1
SLC6A19
- Hartnup disease
SLC7A7
- Lysinuric protein intolerance
SLC7A9
- Cystinuria

11-20

SLC11A1
- Crohn's disease
SLC12A3
- Gitelman syndrome
SLC16A1
- HHF7
SLC16A2
- Allan–Herndon–Dudley syndrome
SLC17A5
- Salla disease
SLC17A8
- DFNA25

21-40

SLC26A2
- Multiple epiphyseal dysplasia 4
- Achondrogenesis type 1B
- Recessive multiple epiphyseal dysplasia
- Atelosteogenesis, type II
- Diastrophic dysplasia
SLC26A4
- Pendred syndrome
SLC35C1
- CDOG 2C
SLC39A4
- Acrodermatitis enteropathica
SLC40A1
- African iron overload

see also solute carrier family

Index of cells

Description	Structure nucleus chromosome genetics Organelles peroxisome cytoskeleton centrosome epithelia cilia mitochondria Membranes proteins cell adhesions 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