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This category reflects the organization of International Statistical Classification of Diseases and Related Health Problems, 10th Revision. Generally, diseases outlined within the ICD-10 codes M60-M79 within Chapter XIII: Diseases of the musculoskeletal system and connective tissue should be included in this category.
Paroxysmal nocturnal dyspnea is a common symptom of several heart conditions such as heart failure with preserved ejection fraction, in addition to asthma, chronic obstructive pulmonary disease, and sleep apnea. [8] Other symptoms that may be seen alongside paroxysmal nocturnal dyspnea are weakness, orthopnea, edema, fatigue, and dyspnea. [9]
ICD-10 is the 10th revision of the International Classification of Diseases (ICD), a medical classification list by the World Health Organization (WHO). It contains codes for diseases, signs and symptoms, abnormal findings, complaints, social circumstances, and external causes of injury or diseases. [1]
Paroxysmal tachycardia is a form of tachycardia which begins and ends in an acute (or paroxysmal) manner. It is also known as Bouveret-Hoffmann syndrome. [ 1 ] [ 2 ] [ 3 ]
unknown, near D20S107 [10] 20p11.2-q13.12 Autosomal recessive dystonia in one family DYT18 612126: SLC2A1: 1p35-p31.3 Paroxysmal exercise-induced dyskinesia DYT19 611031: probably PRRT2: 16q13-q22.1 Episodic kinesigenic dyskinesia 2, probably synonymous with DYT10 DYT20 611147: unknown 2q31 Paroxysmal nonkinesigenic dyskinesia 2 DYT21 614588 ...
Paroxysmal supraventricular tachycardia (PSVT) is a type of supraventricular tachycardia, named for its intermittent episodes of abrupt onset and termination. [3] [6] Often people have no symptoms. [1] Otherwise symptoms may include palpitations, feeling lightheaded, sweating, shortness of breath, and chest pain. [2] The cause is not known. [3]
Tachycardia-induced cardiomyopathy (TIC) is a disease where prolonged tachycardia (a fast heart rate) or arrhythmia (an irregular heart rhythm) causes an impairment of the myocardium (heart muscle), which can result in heart failure.
Cutis laxa may be caused by mutations in the genes: ELN, [8] ATP6V0A2, [9] ATP7A, [10] FBLN4, [11] FBLN5, [12] and PYCR1. [13] A related neurocutaneous syndrome may be caused by mutations in the gene ALDH18A1 (P5CS). [14] Cutis laxa may also be seen in association with inherited connective tissue disorders such as Ehlers–Danlos syndromes.