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.