The following pages link to Naxos syndrome
External toolsShowing 50 items.
View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- Charcot–Marie–Tooth disease (links | edit)
- Lymphedema (links | edit)
- Marfan syndrome (links | edit)
- Mastocytosis (links | edit)
- Ehlers–Danlos syndrome (links | edit)
- Long QT syndrome (links | edit)
- Limb–girdle muscular dystrophy (links | edit)
- Harlequin-type ichthyosis (links | edit)
- Hereditary spherocytosis (links | edit)
- Arrhythmogenic cardiomyopathy (links | edit)
- Naxos disease (redirect page) (links | edit)
- List of diseases (N) (links | edit)
- Keratoderma (links | edit)
- Plakoglobin (links | edit)
- Woolly hair autosomal recessive (links | edit)
- Howel–Evans syndrome (links | edit)
- List of OMIM disorder codes (links | edit)
- List of cutaneous conditions caused by problems with junctional proteins (links | edit)
- Talk:Naxos disease (links | edit)
- User:MastCell/Dermatology Images (links | edit)
- User:PriceDL/List of all WikiProject Medicine articles (links | edit)
- User:CFCF/sandbox/46 (links | edit)
- Misplaced Pages:Reference desk/Archives/Science/2008 May 25 (links | edit)
- Misplaced Pages:WikiProject Medicine/Dermatology task force/Articles created (links | edit)
- Misplaced Pages:WikiProject Medicine/Dermatology task force/Image data (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)
- Hypertrophic cardiomyopathy (links | edit)
- Dilated cardiomyopathy (links | edit)
- Ichthyosis (links | edit)
- Ichthyosis vulgaris (links | edit)
- Lamellar ichthyosis (links | edit)
- Epidermolytic hyperkeratosis (links | edit)
- Epidermolysis bullosa (links | edit)
- Mongolian spot (links | edit)
- Alexander disease (links | edit)
- Usher syndrome (links | edit)
- Gardner's syndrome (links | edit)
- Darier's disease (links | edit)
- Familial adenomatous polyposis (links | edit)
- Port-wine stain (links | edit)
- Keratosis pilaris (links | edit)
- Xeroderma pigmentosum (links | edit)
- Wiskott–Aldrich syndrome (links | edit)
- Incontinentia pigmenti (links | edit)
- Bloom syndrome (links | edit)
- Palmoplantar keratoderma (links | edit)
- Ellis–Van Creveld syndrome (links | edit)
- Ectodermal dysplasia (links | edit)
- Jacobsen syndrome (links | edit)
- X-linked ichthyosis (links | edit)
- Nemaline myopathy (links | edit)
- Connective tissue disease (links | edit)
- Meleda disease (links | edit)
- Giant axonal neuropathy (links | edit)
- Urticaria pigmentosa (links | edit)
- Hereditary elliptocytosis (links | edit)
- Dyskeratosis congenita (links | edit)
- Pseudoxanthoma elasticum (links | edit)
- Nonsyndromic deafness (links | edit)
- Hereditary pyropoikilocytosis (links | edit)
- List of ICD-9 codes 740–759: congenital anomalies (links | edit)
- Tauopathy (links | edit)
- Cutis laxa (links | edit)
- Freeman–Sheldon syndrome (links | edit)
- Dyschromatosis universalis hereditaria (links | edit)