D C167409 ACC/AHA Pediatric and Congenital Cardiology EHR Terminology C26901 Erythema Red discoloration of the skin caused by infectious agents, inflammation, drug hypersensitivity, or underlying disease. Erythema of the palms and/or soles Red discoloration of the skin caused by infectious agents, drug hypersensitivity, or underlying diseases. D C167409 ACC/AHA Pediatric and Congenital Cardiology EHR Terminology C3002 Edema Accumulation of an excessive amount of fluid in cells or intercellular tissues. Edema of the palms and/or soles A clinical finding in which there is the accumulation of excessive fluid in the interstitial spaces, and appears as swelling on visual inspection. A C167409 ACC/AHA Pediatric and Congenital Cardiology EHR Terminology C112180 Acral Erythema Reddening of the palmar and plantar regions of the body with occasional involvement of the distal extremities. Erythema of the palms and/or soles A C167409 ACC/AHA Pediatric and Congenital Cardiology EHR Terminology C157829 Cryoablation for Arrhythmia The use of cold to freeze heart tissue that is a source of an irregular rhythm. It is administered via a balloon catheter that use advanced radiographic techniques. cryoablation A C167409 ACC/AHA Pediatric and Congenital Cardiology EHR Terminology C170883 Acral Edema Accumulation of an excessive amount of watery fluid in cells or intercellular tissues of the hands and feet. Edema of the palms and/or soles A C167409 ACC/AHA Pediatric and Congenital Cardiology EHR Terminology C170884 Cardiac Radiofrequency Ablation The use of radiofrequency energy to destroy an area of heart tissue that is causing an arrhythmia. It is administered via catheterization. radiofrequency ablation A C167409 ACC/AHA Pediatric and Congenital Cardiology EHR Terminology C170885 Neurogenic Orthostatic Hypotension Orthostatic hypotension due to autonomic dysfunction. Primary neurogenic orthostatic hypotension (nOH) may be associated with disorders such as Parkinson disease (PD) and multiple system atrophy (MSA) whereas secondary nOH may be seen in peripheral neuropathies. Neurogenic orthostatic hypotension A C167409 ACC/AHA Pediatric and Congenital Cardiology EHR Terminology C170925 Severity of Chief Complaint Based on Verbal 0-10 Scale The intensity of the chief complaint perceived by the patient as rated using a verbal scale from 0 to 10. Chief Complaint Severity - Verbal 0-10 Scale Verbal 0-10 Scale as appropriate patient's developmental stage. A C167409 ACC/AHA Pediatric and Congenital Cardiology EHR Terminology C170926 Severity of Chief Complaint Based on Wong-Baker Scale The intensity of the chief complaint perceived by the patient as rated using the Wong-Baker Scale (Wong DL, Baker CM. Pain in children: comparison of assessment scales. Pediatr Nurs. 1988;14:9-17). Chief Complaint Severity - Wong-Baker FACES Scale 5- point visual analog scale as appropriate for patient's developmental stage. A C167409 ACC/AHA Pediatric and Congenital Cardiology EHR Terminology C170927 Severity of Chief Complaint Based on Infant FLACC Scale The intensity of the chief complaint perceived by the patient as rated using the Facial expression, Leg movement, Activity, Cry, and Consolability (FLACC) scale (Merkel SI, Voepel-Lewis T, Shayevitz JR, et al. The FLACC: a behavioral scale for scoring postoperative pain in young children. Pediatr Nurs. 1997;23:293-722). Chief Complaint Severity - Infant Behavioral FLACC Scale 0-10 point scale based in caregiver's observation of infant's behavior. M C167409 ACC/AHA Pediatric and Congenital Cardiology EHR Terminology C168046 Psychogenic Musculoskeletal Chest Pain with Dysfunctional Breathing A condition in which there is musculoskeletal chest pain associated with inappropriate hyperpnea or tachypnea. (ACC/AHA) Musculoskeletal chest pain: psychogenic with dysfunctional breathing Musculoskeletal chest pain: psychogenic with hyperventilation A condition in which there is musculoskeletal chest pain associated with inappropriate hyperpnea or tachypnea. M C167409 ACC/AHA Pediatric and Congenital Cardiology EHR Terminology C168045 Musculoskeletal Chest Pain due to Epidemic Myalgia A condition in which there is myositis secondary to an infectious etiology. (ACC/AHA) Musculoskeletal chest pain due to epidemic myalgia Musculoskeletal chest pain due to Bornholm Disease || Musculoskeletal chest pain due to Enterovirus || Musculoskeletal chest pain due to epidemic pleurodynia A condition in which there is myositis secondary to an infectious etiology. M C167409 ACC/AHA Pediatric and Congenital Cardiology EHR Terminology C168333 Musculoskeletal Chest Pain due to Costochondral Junction Syndrome A condition in which there is musculoskeletal chest pain associated with localized inflammation of one or more joints between the rib and the costal cartilage. (ACC/AHA) Musculoskeletal chest pain due to costochondral junction syndrome Tietze A condition in which there is musculoskeletal chest pain associated with localized inflammation of at greater than or equal to 1 joints between the rib and the costal cartilage. M C167409 ACC/AHA Pediatric and Congenital Cardiology EHR Terminology C168392 Precordial Catch Syndrome A condition in which there is musculoskeletal chest pain characterized by brief, sharp discomfort associated with inspiration. (ACC/AHA) Musculoskeletal chest pain: idiopathic/precordial catch syndrome Texidor's twinge A condition in which there is musculoskeletal chest pain characterized by brief, sharp discomfort associated with inspiration. M C167409 ACC/AHA Pediatric and Congenital Cardiology EHR Terminology C2989 22q11.2 Deletion Syndrome A congenital anomaly characterized by immunodeficiency, abnormal facies, congenital heart disease, hypocalcemia, and increased susceptibility to infections. Pathologic characteristics include conotruncal abnormalities and absence or hypoplasia of thymus and parathyroid glands. DiGeorge syndrome is associated with abnormalities of chromosome 22. Also known as DiGeorge anomaly. 22q11 deletion CATCH-22 || DiGeorge syndrome || FACES || Shprintzen syndrome A congenital anomaly characterized by partial deletion of the short arm of chromosome 22. M C167409 ACC/AHA Pediatric and Congenital Cardiology EHR Terminology C84478 Coronary Microvascular Disease A disorder affecting the smallest coronary arteries. Causes include atherosclerosis and arterial spasm. Chest pain is a frequently observed symptom. Microvascular angina Syndrome X A condition in which there is angina pectoris due to occlusion of the smaller coronary arteries. M C167409 ACC/AHA Pediatric and Congenital Cardiology EHR Terminology C84706 Familial Dysautonomia A congenital disorder caused by mutations in the IKBKAP gene. It is characterized by damage of the sympathetic and parasympathetic and sensory nervous system. Familial dysautonomia Riley- Day || hereditary sensory and autonomic neuropathy type III A dysautonomia due to a genetic disorder associated with an abnormality of the sensory and autonomic nerves, decreased sensation of pain and decreased production of tears. M C167409 ACC/AHA Pediatric and Congenital Cardiology EHR Terminology C84909 Multiple System Atrophy A rare neurodegenerative disorder characterized by loss of autonomic nervous system functions and disturbances of motor, balance and muscle coordination. multiple system atrophy Shy-Drager syndrome A condition in which there is neurologic degeneration, postural tachycardia, and muscular rigidity.