Pages that link to "SCN4A"
From WikiMD's Food, Medicine & Wellness Encyclopedia
← SCN4A
The following pages link to SCN4A:
Displayed 50 items.
View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- Neuromyotonia (← links | edit)
- List of OMIM disorder codes (← links | edit)
- Osteopetrosis (← links | edit)
- Liddle syndrome (← links | edit)
- Pseudohypoaldosteronism type 1 (← links | edit)
- Pseudohypoaldosteronism type 2 (← links | edit)
- Myotonia (← links | edit)
- Erythromelalgia (← links | edit)
- Ichthyosis hystrix (← links | edit)
- Clouston's hidrotic ectodermal dysplasia (← links | edit)
- Potassium-aggravated myotonia (← links | edit)
- Spinocerebellar ataxia type 6 (← links | edit)
- Template:Channelopathy (← links | edit)
- Bartter syndrome (← links | edit)
- Benign familial neonatal epilepsy (← links | edit)
- Brugada syndrome (← links | edit)
- Hyperkalemic periodic paralysis (← links | edit)
- Hypoplastic left heart syndrome (← links | edit)
- Central core disease (← links | edit)
- Nephrogenic diabetes insipidus (← links | edit)
- Bart–Pumphrey syndrome (← links | edit)
- Andersen–Tawil syndrome (← links | edit)
- Arrhythmogenic cardiomyopathy (← links | edit)
- Congenital absence of the vas deferens (← links | edit)
- Congenital stationary night blindness (← links | edit)
- Transient neonatal diabetes (← links | edit)
- Paramyotonia congenita (← links | edit)
- Catecholaminergic polymorphic ventricular tachycardia (← links | edit)
- Jervell Lange-Nielsen syndrome (← links | edit)
- Knuckle pads, leuconychia and sensorineural deafness (← links | edit)
- Bartter syndrome type 3 (← links | edit)
- Mucolipidosis type 4 (← links | edit)
- Hypokalemic periodic paralysis (← links | edit)
- Osteopetrosis autosomal dominant type 1 (← links | edit)
- Isaacs' syndrome (← links | edit)
- Becker's myotonia (← links | edit)
- Erythrokeratodermia variabilis et progressiva (← links | edit)
- Ichthyosis hystrix, Curth Macklin type (← links | edit)
- CACNG4 (← links | edit)
- CACNA1G (← links | edit)
- CCDC40 (gene) (← links | edit)
- KCNJ12 (← links | edit)
- UNC13D (← links | edit)
- HOXB2 (← links | edit)
- SCO1 (← links | edit)
- HOXB1 (← links | edit)
- NEUROD2 (← links | edit)
- HOKPP (← links | edit)
- HypoPP (← links | edit)
- HypoKPP (← links | edit)