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Template
:
Channelopathy
From WikiMD's Medical Encyclopedia
Diseases of ion channels
Calcium channel
Voltage-gated
*
CACNA1A
Familial hemiplegic migraine 1
Episodic ataxia 2
Spinocerebellar ataxia type-6
CACNA1C
Timothy syndrome
Brugada syndrome 3
Long QT syndrome 8
CACNA1F
Ocular albinism 2
CSNB2A
CACNA1S
Hypokalemic periodic paralysis 1
Thyrotoxic periodic paralysis 1
CACNB2
Brugada syndrome 4
Ligand gated
*
RYR1
Malignant hyperthermia
Central core disease
RYR2
CPVT1
ARVD2
Sodium channel
Voltage-gated
*
SCN1A
Familial hemiplegic migraine 3
GEFS+ 2
Febrile seizure 3A
SCN1B
Brugada syndrome 6
GEFS+ 1
SCN4A
Hypokalemic periodic paralysis 2
Hyperkalemic periodic paralysis
Paramyotonia congenita
Potassium-aggravated myotonia
SCN4B
Long QT syndrome 10
SCN5A
Brugada syndrome 1
Long QT syndrome 3
SCN9A
Erythromelalgia
Febrile seizure 3B
Paroxysmal extreme pain disorder
Congenital insensitivity to pain
Constitutively active
*
SCNN1B
/
SCNN1G
Liddle's syndrome
SCNN1A
/
SCNN1B
/
SCNN1G
Pseudohypoaldosteronism 1AR
Potassium channel
Voltage-gated
*
KCNA1
Episodic ataxia 1
KCNA5
Familial atrial fibrillation 7
KCNC3
Spinocerebellar ataxia type-13
KCNE1
Jervell and Lange-Nielsen syndrome
Long QT syndrome 5
KCNE2
Long QT syndrome 6
KCNE3
Brugada syndrome 5
KCNH2
Short QT syndrome
KCNQ1
Jervell and Lange-Nielsen syndrome
Romano–Ward syndrome
Short QT syndrome
Long QT syndrome 1
Familial atrial fibrillation 3
KCNQ2
BFNS1
Inward-rectifier
*
KCNJ1
Bartter syndrome 2
KCNJ2
Andersen–Tawil syndrome
Long QT syndrome 7
Short QT syndrome
KCNJ11
TNDM3
KCNJ18
Thyrotoxic periodic paralysis 2
Chloride channel
*
CFTR
Cystic fibrosis
Congenital absence of the vas deferens
CLCN1
Thomsen disease
Myotonia congenita
CLCN5
Dent's disease
CLCN7
Osteopetrosis A2, B4
BEST1
Vitelliform macular dystrophy
CLCNKB
Bartter syndrome 3
TRP channel
*
TRPC6
FSGS2
TRPML1
Mucolipidosis type IV
See also:
ion channels
Categories
:
Channelopathies
Genetic disease and disorder templates by mechanism
