ACHROMATOPSIA 3
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ATRIAL FIBRILLATION, FAMILIAL, 10, INCLUDED
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ATRIAL FIBRILLATION, FAMILIAL, 7
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ATRIAL STANDSTILL, INCLUDED;;
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BRACHYOLMIA TYPE 3
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BRUGADA SYNDROME 1
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BRUGADA SYNDROME 1, INCLUDED;;
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CARDIAC CONDUCTION DEFECT, NONSPECIFIC, INCL
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CARDIOMYOPATHY, DILATED, 1E
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CENTRAL CORE DISEASE
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CENTRAL CORE DISEASE, AUTOSOMAL RECESSIVE
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DEAFNESS, AUTOSOMAL DOMINANT 2A
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DRAVET SYNDROME
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EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 6
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EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 6
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EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 11, MILD
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EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 13
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EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 6
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EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 7
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EPISODIC ATAXIA, TYPE 1
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EPISODIC ATAXIA, TYPE 2
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EPISODIC ATAXIA, TYPE 2, INCLUDED
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EPISODIC PAIN SYNDROME, FAMILIAL, 1
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EPISODIC PAIN SYNDROME, FAMILIAL, 2
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ERYTHERMALGIA, PRIMARY
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FACIES
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GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 2
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GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 2, INCLUDED
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HEREDITARY MOTOR AND SENSORY NEUROPATHY, TYPE IIC
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HYPERKALEMIC PERIODIC PARALYSIS
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HYPOKALEMIC PERIODIC PARALYSIS, TYPE 1
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HYPOKALEMIC PERIODIC PARALYSIS, TYPE 2
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HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC
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INCLUDED;;
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INSENSITIVITY TO PAIN, CHANNELOPATHY-ASSOCIATED
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LONG QT SYNDROME 2
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LONG QT SYNDROME 3
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LONG QT SYNDROME 3/6, DIGENIC, INCLUDED
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LONG QT SYNDROME, BRADYCARDIA-INDUCED
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MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 1
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MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 1, INCLUDED
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MIGR
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MIGRAINE, FAMILIAL HEMIPLEGIC 1, WITH PROGRESSIVE CEREBELLAR ATAXIA
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MIGRAINE, FAMILIAL HEMIPLEGIC 1, WITH PROGRESSIVE CEREBELLAR ATAXIA,
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MIGRAINE, FAMILIAL HEMIPLEGIC, 1
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MINICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA, INCLUDED
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MYASTHENIC SYNDROME, CONGENITAL, ACETAZOLAMIDE-RESPONSIVE
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MYOKYMIA 1
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MYOKYMIA 1 WITH HYPOMAGNESEMIA
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MYOTONIA CONGENITA, ATYPICAL
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MYOTONIA CONGENITA, ATYPICAL, ACETAZOLAMIDE-RESPONSIVE
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MYOTONIA, POTASSIUM-AGGRAVATED
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NEUROMUSCULAR DISEASE, CONGENITAL, WITH UNIFORM TYPE 1 FIBER, INCLUDED
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NEUROPATHY, SMALL FIBER
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NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1C
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NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A
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NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A, SEVERE
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NORMOKALEMIC PERIODIC PARALYSIS, POTASSIUM-SENSITIVE
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PALMOPLANTAR KERATODERMA, MUTILATING, WITH PERIORIFICIAL KERATOTIC
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PARAMYOTONIA CONGENITA
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PARAMYOTONIA CONGENITA, INCLUDED
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PARAMYOTONIA CONGENITA/HYPERKALEMIC PERIODIC PARALYSIS
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PARAMYOTONIA CONGENITA/HYPERKALEMIC PERIODIC PARALYSIS, INCLUDED
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PARASTREMMATIC DWARFISM, INCLUDED
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PAROXYSMAL EXTREME PAIN DISORDER
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PLAQUES
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POLYCYSTIC KIDNEY DISEASE 2
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PRIMARY ALDOSTERONISM, SEIZURES, AND NEUROLOGIC ABNORMALITIES
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PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IA
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RETINAL CONE DYSTROPHY 3B
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RETINITIS PIGMENTOSA 49
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ROD MONOCHROMACY
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SEIZURES, BENIGN FAMILIAL INFANTILE, 3
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SEIZURES, BENIGN FAMILIAL NEONATAL, 1
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SEIZURES, BENIGN FAMILIAL NEONATAL, 1, AND/OR MYOKYMIA
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SEIZURES, BENIGN FAMILIAL NEONATAL, 2
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SHORT QT SYNDROME 1
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SICK SINUS SYNDROME 1, AUTOSOMAL RECESSIVE
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SICK SINUS SYNDROME 2, AUTOSOMAL DOMINANT
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SKIN/HAIR/EYE PIGMENTATION 10, BLOND/BROWN HAIR
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SPINOCEREBELLAR ATAXIA 13
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SPINOCEREBELLAR ATAXIA 19
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SPINOCEREBELLAR ATAXIA 6
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SPINOCEREBELLAR ATAXIA 6, INCLUDED
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SPONDYLOEPIPHYSEAL DYSPLASIA, MAROTEAUX TYPE
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SPONDYLOMETAPHYSEAL DYSPLASIA, KOZLOWSKI TYPE
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TIMOTHY SYNDROME
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VARIANT OF UNKNOWN SIGNIFICANCE
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VENTRICULAR FIBRILLATION, PAROXYSMAL FAMILIAL
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VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1
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