The following pages link to Congenital hereditary endothelial dystrophy
External toolsShowing 34 items.
View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- Fuchs' dystrophy (links | edit)
- Corneal dystrophy (links | edit)
- Meesmann corneal dystrophy (links | edit)
- Macular corneal dystrophy (links | edit)
- Reis–Bucklers corneal dystrophy (links | edit)
- Thiel–Behnke dystrophy (links | edit)
- X-linked endothelial corneal dystrophy (links | edit)
- Posterior polymorphous corneal dystrophy (links | edit)
- Congenital endothelial dystrophy type 1 (redirect page) (links | edit)
- Talk:Congenital endothelial dystrophy type 1 (links | edit)
- User:CopperKettle (links | edit)
- User:AlexNewArtBot/MedicineSearchResult/archive22 (links | edit)
- User:PriceDL/List of all WikiProject Medicine articles (links | edit)
- User:CFCF/sandbox/46 (links | edit)
- User talk:X!/Archives/2/2011 (links | edit)
- User talk:X!/Archives/8/2011 (links | edit)
- User talk:X!/Archives/11/2011 (links | edit)
- Misplaced Pages:WikiProject Medicine/Lists of pages/Articles (links | edit)
- Misplaced Pages:WikiProject Medicine/Lists of pages/NA-, ???-importance medicine articles (links | edit)
- Misplaced Pages:WikiProject Medicine/Popular pages En 2013b (links | edit)
- Congenital endothelial dystrophy type 2 (redirect page) (links | edit)
- Boron (links | edit)
- Genetic disorder (links | edit)
- Crohn's disease (links | edit)
- Congenital disorder of glycosylation (links | edit)
- Fructose malabsorption (links | edit)
- Hyperinsulinemic hypoglycemia (links | edit)
- Cystinuria (links | edit)
- Pendred syndrome (links | edit)
- Diastrophic dysplasia (links | edit)
- Atelosteogenesis, type II (links | edit)
- Fuchs' dystrophy (links | edit)
- Gitelman syndrome (links | edit)
- Hartnup disease (links | edit)
- Salla disease (links | edit)
- Lysinuric protein intolerance (links | edit)
- Hereditary elliptocytosis (links | edit)
- Achondrogenesis type 1B (links | edit)
- African iron overload (links | edit)
- Nonsyndromic deafness (links | edit)
- Autosomal recessive multiple epiphyseal dysplasia (links | edit)
- Acrodermatitis enteropathica (links | edit)
- Testicular microlithiasis (links | edit)
- Solute carrier family (links | edit)
- Multiple epiphyseal dysplasia (links | edit)
- Episodic ataxia (links | edit)
- Thyroid dyshormonogenesis (links | edit)
- Arterial tortuosity syndrome (links | edit)
- Renal glycosuria (links | edit)
- Allan–Herndon–Dudley syndrome (links | edit)
- GLUT1 deficiency (links | edit)
- Glucose-galactose malabsorption (links | edit)
- Sodium bicarbonate transporter-like protein 11 (links | edit)
- Mitochondrial pyruvate carrier 2 (links | edit)
- Monocarboxylate transporter 1 (links | edit)
- Fanconi–Bickel syndrome (links | edit)
- Inborn errors of carbohydrate metabolism (links | edit)
- Iminoglycinuria (links | edit)
- Ichthyosis prematurity syndrome (links | edit)
- Congenital disorder of glycosylation type IIc (links | edit)
- SLC17A3 (links | edit)
- Mitochondrial pyruvate carrier 1 (links | edit)
- SPATCCM (links | edit)
- Talk:Congenital endothelial dystrophy type 2 (links | edit)
- User:CopperKettle (links | edit)
- User:AlexNewArtBot/GeneticsSearchResult/archive1 (links | edit)
- User:AlexNewArtBot/AcademicSearchResult/archive5 (links | edit)
- User:AlexNewArtBot/OrganizationsSearchResult/archive47 (links | edit)
- User:AlexNewArtBot/MedicineSearchResult/archive22 (links | edit)
- User:PriceDL/List of all WikiProject Medicine articles (links | edit)
- User:CFCF/sandbox/46 (links | edit)
- User talk:X!/Archives/5/2011 (links | edit)
- Misplaced Pages:WikiProject Medicine/Lists of pages/Articles (links | edit)
- Misplaced Pages:WikiProject Medicine/Lists of pages/NA-, ???-importance medicine articles (links | edit)
- Misplaced Pages:WikiProject Medicine/Popular pages En 2013b (links | edit)
- Template:Solute carrier disorders (links | edit)
- Congenital stromal corneal dystrophy (links | edit)
- Posterior amorphous corneal dystrophy (links | edit)
- Schnyder crystalline corneal dystrophy (links | edit)
- Fleck corneal dystrophy (links | edit)
- Lisch epithelial corneal dystrophy (links | edit)
- Subepithelial mucinous corneal dystrophy (links | edit)
- Gelatinous drop-like corneal dystrophy (links | edit)
- Epithelial basement membrane dystrophy (links | edit)
- Lattice corneal dystrophy (links | edit)
- Granular corneal dystrophy (links | edit)
- Congenital endothelial dystrophy (redirect page) (links | edit)
- Corneal opacity (links | edit)
- Talk:Congenital hereditary endothelial dystrophy (transclusion) (links | edit)
- User:MastCell/Ignored medical articles (links | edit)
- User:PriceDL/List of all WikiProject Medicine articles (links | edit)
- User:CFCF/sandbox/46 (links | edit)
- User:Klundern/sandbox (links | edit)
- User:Klundern/Macular Corneal Dystrophy (links | edit)
- User:Klundern/Distrofia Macular Corneal (links | edit)
- Misplaced Pages:WikiProject Medicine/Lists of pages/Articles (links | edit)
- Misplaced Pages:WikiProject Medicine/Lists of pages/Low-importance medicine articles (links | edit)
- Misplaced Pages:WikiProject Medicine/Popular pages En 2013b (links | edit)
- Misplaced Pages:WikiProject Medicine/The ICD-11 coding challenge/6000–6099 (links | edit)
- Template:Human corneal dystrophy (links | edit)