SLC35C1
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Congenital disorder of glycosylation — Congenital disorders of glycosylation Classification and external resources ICD 10 E77.8 ICD 9 271.8 … Wikipedia
Congenital disorder of glycosylation type IIc — Classification and external resources OMIM 266265 Congenital disorder of glycosylation type IIc or Leukocyte adhesion deficiency 2 (LAD2) is a type of leukocyte adhesion deficiency attributable to the absence of neutrophil sialyl LewisX, a ligand … Wikipedia
Genetic disorder — For a non technical introduction to the topic, see Introduction to genetics. Genetic disorder Classification and external resources MeSH D030342 A genetic disorder is an illness caused by abnormalities in genes or … Wikipedia
Membrane transport protein — A membrane transport protein (or simply transporter) is a membrane protein[1] involved in the movement of ions, small molecules, or macromolecules, such as another protein across a biological membrane. Transport proteins are integral membrane… … Wikipedia
Fructose malabsorption — Classification and external resources Fructose ICD 10 E … Wikipedia
Cystinuria — Classification and external resources Chemical structure of cystine formed from L cysteine (under biological conditions) ICD 10 E … Wikipedia
Pendred syndrome — Classification and external resources OMIM 274600 DiseasesDB 9771 GeneReviews … Wikipedia
Diastrophic dysplasia — Classification and external resources OMIM 222600 DiseasesDB 30759 eMedicine … Wikipedia
Fuchs' dystrophy — Classification and external resources Fuchs corneal dystrophy. Light microscopic appearance of the cornea showing numerous excrescences (guttae) on the posterior surface of Descemet s membrane and the presence of cysts in the corneal epithelium… … Wikipedia
Dopamine transporter — Solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 Identifiers Symbols … Wikipedia