The following pages link to PCNT
External toolsShowing 50 items.
View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- Centriole (links | edit)
- Charcot–Marie–Tooth disease (links | edit)
- Red panda (links | edit)
- Marfan syndrome (links | edit)
- Centrosome (links | edit)
- Long QT syndrome (links | edit)
- Limb–girdle muscular dystrophy (links | edit)
- Hereditary spherocytosis (links | edit)
- Arrhythmogenic cardiomyopathy (links | edit)
- Hypertrophic cardiomyopathy (links | edit)
- Dilated cardiomyopathy (links | edit)
- Epidermolytic hyperkeratosis (links | edit)
- Alexander disease (links | edit)
- Usher syndrome (links | edit)
- Gardner's syndrome (links | edit)
- Familial adenomatous polyposis (links | edit)
- Wiskott–Aldrich syndrome (links | edit)
- Palmoplantar keratoderma (links | edit)
- Nemaline myopathy (links | edit)
- Giant axonal neuropathy (links | edit)
- Hereditary elliptocytosis (links | edit)
- Chromosome 21 (links | edit)
- Nonsyndromic deafness (links | edit)
- Hereditary pyropoikilocytosis (links | edit)
- Tauopathy (links | edit)
- Freeman–Sheldon syndrome (links | edit)
- Larsen syndrome (links | edit)
- Epidermolysis bullosa simplex (links | edit)
- Primordial dwarfism (links | edit)
- Emery–Dreifuss muscular dystrophy (links | edit)
- Short rib–polydactyly syndrome (links | edit)
- White sponge nevus (links | edit)
- MASS syndrome (links | edit)
- Naegeli–Franceschetti–Jadassohn syndrome (links | edit)
- Laminopathy (links | edit)
- Monilethrix (links | edit)
- May–Hegglin anomaly (links | edit)
- Congenital contractural arachnodactyly (links | edit)
- Buschke–Ollendorff syndrome (links | edit)
- Barraquer–Simons syndrome (links | edit)
- Pelger–Huët anomaly (links | edit)
- Steatocystoma multiplex (links | edit)
- PCM1 (links | edit)
- Ninein (links | edit)
- CENPJ (links | edit)
- CEP350 (links | edit)
- Osteopoikilosis (links | edit)
- PIBF1 (links | edit)
- CEP55 (links | edit)
- CKAP5 (links | edit)