Pages that link to "Gigaxonin"
From WikiMD's Food, Medicine & Wellness Encyclopedia
The following pages link to Gigaxonin:
Displayed 50 items.
View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- Laminopathy (← links | edit)
- Keratin 14 (← links | edit)
- Hereditary spherocytosis (← links | edit)
- Hereditary elliptocytosis (← links | edit)
- Usher syndrome (← links | edit)
- Nemaline myopathy (← links | edit)
- White sponge nevus (← links | edit)
- Alexander disease (← links | edit)
- Reticular pigmented anomaly of the flexures (← links | edit)
- Ichthyosis hystrix (← links | edit)
- May–Hegglin anomaly (← links | edit)
- Wiskott–Aldrich syndrome (← links | edit)
- Barraquer-Simons syndrome (← links | edit)
- Boomerang dysplasia (← links | edit)
- Buschke Ollendorff syndrome (← links | edit)
- Marfan syndrome (← links | edit)
- Monilethrix (← links | edit)
- Limb-girdle muscular dystrophy (← links | edit)
- FG syndrome (← links | edit)
- Familial adenomatous polyposis (← links | edit)
- Epidermolysis bullosa simplex (← links | edit)
- Congenital contractural arachnodactyly (← links | edit)
- Template:Cytoskeletal defects (← links | edit)
- Template:Cytoskeletal proteins (← links | edit)
- Familial hypertrophic cardiomyopathy (← links | edit)
- Wiskott Aldrich syndrome (← links | edit)
- MYH9 related thrombocytopenia (← links | edit)
- Buschke–Ollendorff syndrome (← links | edit)
- Arrhythmogenic cardiomyopathy (← links | edit)
- Asphyxiating thoracic dysplasia (← links | edit)
- Charcot–Marie–Tooth disease (← links | edit)
- Emery–Dreifuss muscular dystrophy (← links | edit)
- Weill–Marchesani syndrome (← links | edit)
- Microcephalic osteodysplastic primordial dwarfism type II (← links | edit)
- Pelger–Huët anomaly (← links | edit)
- Naxos syndrome (← links | edit)
- Gardner syndrome (← links | edit)
- Usher syndrome, type 1 (← links | edit)
- Usher syndrome type 2A (← links | edit)
- Familial partial lipodystrophy type 2 (← links | edit)
- Charcot-Marie-Tooth disease (← links | edit)
- Limb-girdle muscular dystrophy type 2I (← links | edit)
- Limb-girdle muscular dystrophy, type 2C (← links | edit)
- Epidermolysa bullosa simplex with muscular dystrophy (← links | edit)
- Limb-girdle muscular dystrophy type 2A (← links | edit)
- Limb-girdle muscular dystrophy type 2B (← links | edit)
- Intermediate congenital nemaline myopathy (← links | edit)
- Epidermolysis bullosa simplex, Dowling-Meara type (← links | edit)
- Epidermolysis bullosa simplex, generalized (← links | edit)
- Epidermolysis bullosa simplex, localized (← links | edit)
