basal heart rate; benign hypertrophic prostatitis; bronchial hyperreactivity
 

 
Chronic hypertrophic rhinitis
 

 
Hypertrophic Cardio-Myopathy
  = HCMP
 

 
Familial Hypertrophic Cardiomyopathy
 

 
Hypertrophic Cardiomyopathy
 

 
Hypertrophic Cardiomyopathy
 

 
hypertrophic cardiomyopathy
 

 
Hypertrophic non-obstructive cardiomyopathy
 

비대성 관절염

비후성 반흔

증식성 치은염

비대성 폐쇄성 심근병증

비후성 폐 골관절병증

비후성 비염

비후성 난관염

만성 비후 인두염, 만성 비후성 인두염

특발성 과형성 골관절병증

속발성 비대성 골 관절병증

비대층

비후성 편평 태선

비후성 루푸스

 
A myocardial disease characterised by hypertrophy, involving mainly the interventricular septum, interfering with left ventricular emptying.
(12 Dec 1998)
 

 
Swelling of the vulval tissues due to lymphatic obstruction; in some cases it may be caused by filariasis, with induration or ulceration of the skin.
Synonym: elephantiasis vulvae.
(05 Mar 2000)
 

 
dejerine-Sottas disease
 

 
An elevated scar, resembling a keloid, but which does not spread into surrounding tissues. It is formed by enlargement and overgrowth of cicatricial tissue and regresses spontaneously.
(12 Dec 1998)
 

 
Familial occurrence of hypertrophic cardiomyopathy exhibiting an autosomal dominant pattern of inheritance. Familial cardiomyopathy of various kinds occurs with autosomal dominant inheritance. There is also an asymmetrical form affecting the ventricles and the interventricular septum.
(05 Mar 2000)
 

 
Gastritis with hypertrophy of gastric mucosa folds. Symptoms include vomiting, diarrhoea, weight loss, excessive mucus secretion, and hypoproteinaemia.
(12 Dec 1998)
 

 
dejerine-Sottas disease
 

 
<cardiology> A congenital heart disease that results in abnormal thickening of the ventricular septum and left ventricular wall. Enlargement of the ventricular septum can result in ventricular outflow obstruction (subaortic stenosis) and eventual cardiomyopathy.
(27 Sep 1997)
 

 
A conditioned chiefly characterised by thickening of the skin of the head and distal extremities, deep folds and furrows of the skin of the forehead, cheeks, and scalp, seborrhoea, hyperhidrosis, periostosis of the long bones, digital clubbing, and spadelike enlargement of the hands and feet. It is more prevalent in the male, and is usually first evident during adolescence. It is believed to be inherited as an autosomal dominant trait.
(12 Dec 1998)
 

 
Symmetrical osteitis of the four limbs, chiefly localised to the phalanges and the terminal epiphyses of the long bones of the forearm and leg, sometimes extending to the proximal ends of the limbs and the flat bones, and accompanied by dorsal kyphosis and joint involvement. It is often secondary to chronic conditions of the lungs and heart.
(12 Dec 1998)
 

 
A familial type of demyelinating sensorimotor polyneuropathy that begins in early childhood and is slowly progressive; clinically characterised by foot pain and paresthesias, followed by symmetrical weakness and wasting of the distal limbs; one of the causes of stork legs; patients are wheelchair bound at an early age; peripheral nerves are palpably enlarged and non-tender; pathologically, onion bulb formation is seen in the nerves: whorls of overlapping, intertwined Schwann cell processes that encircle bare axons; usually autosomal recessive inheritance.
Synonym: Dejerine's disease, progressive hypertrophic polyneuropathy.
(05 Mar 2000)
 

 
Acne vulgaris in which the lesions, on healing, leave hypertrophic scars.
(05 Mar 2000)
 

 
Thickening of skin with accentuated skin lines in eczema.
Synonym: chronic eczema, eczema hypertrophicum.
(05 Mar 2000)
 

 
Verrucoid or warty lesions occurring on legs and thighs in association with lichen planus elsewhere.
Synonym: lichen planus verrucosus, lichen ruber verrucosus.
(05 Mar 2000)
 

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성분/함량

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