The following pages link to Galactosylceramide
External toolsShowing 13 items.
View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- List of MeSH codes (D02) (links | edit)
- Galactosylceramidase (links | edit)
- CD1D (links | edit)
- Galactosylceramides (redirect page) (links | edit)
- Galactosylceramide sulfotransferase (links | edit)
- Glycoside hydrolase family 59 (links | edit)
- Galactocerebroside (redirect page) (links | edit)
- Lipid (links | edit)
- Myelin (links | edit)
- Canavan disease (links | edit)
- Pelizaeus–Merzbacher disease (links | edit)
- Tay–Sachs disease (links | edit)
- Gaucher's disease (links | edit)
- Lysosomal storage disease (links | edit)
- Niemann–Pick disease (links | edit)
- Glycolipid (links | edit)
- Sphingolipid (links | edit)
- Sphingomyelin (links | edit)
- Sphingosine (links | edit)
- Glycosphingolipid (links | edit)
- Ganglioside (links | edit)
- Krabbe disease (links | edit)
- GD2 (links | edit)
- Batten disease (links | edit)
- Neuronal ceroid lipofuscinosis (links | edit)
- Metachromatic leukodystrophy (links | edit)
- Infantile neuronal ceroid lipofuscinosis (links | edit)
- Inborn error of lipid metabolism (links | edit)
- Ceramide (links | edit)
- Sandhoff disease (links | edit)
- GM2-gangliosidosis, AB variant (links | edit)
- Cerebroside (links | edit)
- Glycan (links | edit)
- Gangliosidosis (links | edit)
- Lipid storage disorder (links | edit)
- Farber disease (links | edit)
- Glucocerebroside (links | edit)
- List of ICD-9 codes 240–279: endocrine, nutritional and metabolic diseases, and immunity disorders (links | edit)
- Glycoconjugate (links | edit)
- Sphingolipidoses (links | edit)
- GM2 gangliosidoses (links | edit)
- GM1 gangliosidoses (links | edit)
- GM1 (links | edit)
- Mucolipidosis type IV (links | edit)
- Sulfatide (links | edit)
- Cerebrotendinous xanthomatosis (links | edit)
- Sphingosine-1-phosphate (links | edit)
- Galactosylceramide (links | edit)
- Globoside (links | edit)
- Prosaposin (links | edit)
- Myelinogenesis (links | edit)
- UGT8 (links | edit)
- Multiple sulfatase deficiency (links | edit)
- GM2 (ganglioside) (links | edit)
- Jansky–Bielschowsky disease (links | edit)
- Metabolic intermediate (links | edit)
- Sulfatidosis (links | edit)
- Niemann–Pick disease type C (links | edit)
- SMPD1-associated Niemann–Pick disease (links | edit)
- Globotriaosylceramide (links | edit)
- Lactosylceramide (links | edit)
- Galactolipid (links | edit)
- Lysosomal acid lipase deficiency (links | edit)
- Stage-specific embryonic antigen 3 (links | edit)
- GM3 (links | edit)
- Lipidology (links | edit)
- Forssman antigen (links | edit)
- Siponimod (links | edit)
- Globo H (links | edit)
- Talk:Brain/Archive 2 (links | edit)
- Talk:Galactosylceramide (links | edit)
- Talk:Galactocerebroside (transclusion) (links | edit)
- User:ShieldsMU/sandbox (links | edit)
- User:7753spoom/sandbox/Sulfatide (links | edit)
- User:Y-S.Ko/Wikipedia course/Diseases (links | edit)
- User talk:Ebe123/News (links | edit)
- Misplaced Pages:WikiProject Pharmacology/Log/2011-05-05 (links | edit)
- Template:Sphingolipids (links | edit)
- Template:Lipid storage disorders (links | edit)
- Category:Lipid storage disorders (links | edit)
- Galactosyl ceramide (redirect page) (links | edit)
- Combined Saposin Deficiency (links | edit)
- Talk:Galactosylceramide (transclusion) (links | edit)
- Misplaced Pages:WikiProject Chemistry/Lists of pages/Chemistry all pages (links | edit)
- Misplaced Pages:WikiProject Chemistry/Lists of pages/Chemistry articles (links | edit)
- Draft:Combined Saposin Deficiency (links | edit)