ABCA12	ATP-binding cassette transporter A12
ABHD5	α/β hydrolase domain containing protein 5
ARS	Syndrome arthrogryposis, renal dysfunction and cholestasis
LD	Linear dichroism
ASPRV1	Aspartic peptidase, retroviral-like 1
CaR	Calcium-sensing receptor
CE	Cornified envelope
CGI58	Comparative gene identification-58
CHILD syndrome	Congenital hemidysplasia with ichthyosiform erythroderma and limb defects
CLSP	Calmodulin-like skin protein
Cystatin A	Cysteine protease inhibitor A
Cx26	Connexin 26
ELOVL	Fatty acid elongases
FATP4	Fatty acid transport protein 4
GJB2/GJB6	Gap junction protein beta 2/gap junction protein beta 6
KID	Keratitis-ichthyosis-deafness
KLK	Kallikrein-related peptidase
LEKTI	Lymphoepithelial-Kazal-type 5 inhibitor
LXR	Liver X receptor
NIPAL4	NIPA like domain containing 4
NSDHL	NADP dependent steroid dehydrogenase-like
Orai1	ORAI calcium release-activated calcium modulator 1
PNPLA1	Patatin-like phospholipase domain-containing lipase 1
PPAR	Peroxisome proliferating activated receptor
SAM	Syndrome severe skin dermatitis, multiple allergies, and metabolic wasting
SASPase	Skin aspartic protease
SC	Stratum corneum
SDR9C7	Short-chain dehydrogenase/reductase family 9C member 7
SGMS	Sphingomyelin synthase
SOCE	Store-operated calcium entry
SPINK5	Serine-specific inhibitor Kazal type 5
SPRR	Small proline-rich protein
STIM1	Stromal interaction molecule1
TGases	Transglutaminases
TSLP	Thymic stromal lymphoprotein
TRP	Transient receptor potential
TRPV	TRP vanilloid type
UGCG	UDP-glucose:ceramide glucosyltransferase