Pages that link to "SCN5A"
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← SCN5A
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- Genetic disorder (links | edit)
- Methadone (links | edit)
- Neuromyotonia (links | edit)
- Cystic fibrosis (links | edit)
- Febrile seizure (links | edit)
- Brugada syndrome (links | edit)
- Irritable bowel syndrome (links | edit)
- Long QT syndrome (links | edit)
- Sinus node dysfunction (links | edit)
- Osteopetrosis (links | edit)
- Arrhythmogenic cardiomyopathy (links | edit)
- Dilated cardiomyopathy (links | edit)
- Congenital insensitivity to pain (links | edit)
- Malignant hyperthermia (links | edit)
- Erythromelalgia (links | edit)
- Cardiac action potential (links | edit)
- Hallermann–Streiff syndrome (links | edit)
- Hyperkalemic periodic paralysis (links | edit)
- Timothy syndrome (links | edit)
- Jervell and Lange-Nielsen syndrome (links | edit)
- Romano–Ward syndrome (links | edit)
- Andersen–Tawil syndrome (links | edit)
- Hypoplastic left heart syndrome (links | edit)
- Channelopathy (links | edit)
- Myotonia congenita (links | edit)
- Hypokalemic periodic paralysis (links | edit)
- Paramyotonia congenita (links | edit)
- Chromosome 3 (links | edit)
- Nephrogenic diabetes insipidus (links | edit)
- Liddle's syndrome (links | edit)
- Bartter syndrome (links | edit)
- Ion transporter (links | edit)
- Vitelliform macular dystrophy (links | edit)
- PDZ domain (links | edit)
- Congenital absence of the vas deferens (links | edit)
- Desmoglein-2 (links | edit)
- Pseudohypoaldosteronism (links | edit)
- Mucolipidosis type IV (links | edit)
- EF hand (links | edit)
- Generalized epilepsy with febrile seizures plus (links | edit)
- SCN5A (transclusion) (links | edit)
- Ajmaline (links | edit)
- Benign familial neonatal seizures (links | edit)
- Catecholaminergic polymorphic ventricular tachycardia (links | edit)
- Spinocerebellar ataxia type 6 (links | edit)
- Episodic ataxia (links | edit)
- Spinocerebellar ataxia type-13 (links | edit)
- Congenital stationary night blindness (links | edit)
- Familial atrial fibrillation (links | edit)
- Dent's disease (links | edit)