cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome
Also known as: CAGSSS, cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia
Additional Disease Briefs
cataract-hypertrichosis-intellectual disability syndrome
Also known as: CAHMR syndrome, cataract, hypertrichosis, intellectual disability syndrome, cataract, hypertrichosis, mental retardation syndrome
catastrophic antiphospholipid syndrome
Also known as: CAPS, caps, catastrophic APS
catecholaminergic polymorphic ventricular tachycardia
Also known as: CPVT, bidirectional tachycardia induced by catecholamine, catecholamine-induced polymorphic ventricular tachycardia, catecholaminergic polymorphic ventricular tachycardia, double tachycardia induced by catecholamines, familial polymorphic ventricular tachycardia, malignant paroxysmal ventricular tachycardia, multifocal ventricular premature beats, polymorphic catecholergic ventricular tachycardia, stress-induced polymorphic ventricular tachycardia, syncopal paroxysmal tachycardia, ventricular tachycardia, catecholaminergic polymorphic
catecholaminergic polymorphic ventricular tachycardia 1
Also known as: ARVC2, ARVD2, CPVT1, CVPT1, RYR2 familial isolated arrhythmogenic right ventricular dysplasia, arrhythmogenic right ventricular cardiomyopathy 2, arrhythmogenic right ventricular dysplasia 2, arrhythmogenic right ventricular dysplasia type 2, arrhythmogenic right ventricular dysplasia, familial, 2, arrhythmogenic right ventricular dysplasia, familial, type 2, catecholaminergic polymorphic ventricular tachycardia 1, catecholaminergic polymorphic ventricular tachycardia type 1, familial arrhythmogenic right ventricular dysplasia 2, familial isolated arrhythmogenic right ventricular dysplasia caused by mutation in RYR2, ventricular tachycardia, catecholaminergic polymorphic, 1, ventricular tachycardia, catecholaminergic polymorphic, 1, with or without atrial dysfunction and/or dilated cardiomyopathy, ventricular tachycardia, stress-induced polymorphic
catecholaminergic polymorphic ventricular tachycardia 3
Also known as: CPVT3, CVPT3, TECRL catecholaminergic polymorphic ventricular tachycardia, catecholaminergic polymorphic ventricular tachycardia 3, catecholaminergic polymorphic ventricular tachycardia caused by mutation in TECRL, catecholaminergic polymorphic ventricular tachycardia type 3, ventricular tachycardia, catecholaminergic polymorphic, 3
catecholaminergic polymorphic ventricular tachycardia 5
Also known as: CPVT5, CVPT5, TRDN catecholaminergic polymorphic ventricular tachycardia, cardiac arrhythmia syndrome, with or without skeletal muscle weakness, catecholaminergic polymorphic ventricular tachycardia 5, catecholaminergic polymorphic ventricular tachycardia caused by mutation in TRDN, catecholaminergic polymorphic ventricular tachycardia type 5, ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness
cathepsin a-related arteriopathy-strokes-leukoencephalopathy
Also known as: CARASAL
caudal duplication
Also known as: caudal DUPLICATION anomaly, dipygus, split notochord syndrome