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  • immunodeficiency syndrome, combine
    º¹ÇÕÇü ¸é¿ª°áÇÌ Áõ (Èıº)
  • immunodeficiency syndrome, congenital
    ¼±Ãµ¼º ¸é¿ª°áÇÌ ÁõÈıº
  • immunodeficiency syndrome, primary
    ÀÏÂ÷¼º ¸é¿ª°áÇÌ ÁõÈıº, ¿ø¹ß¼º ¸é¿ª°áÇÌ ÁõÈıº
  • immunodeficiency syndrome, secondary
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  • immunodeficiency syndrome, severe combined
    ÁßÁõº¹ÇÕÇü ¸é¿ª°áÇÌ ÁõÈıº
  • primary immunodeficiency
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  • primary immunodeficiency syndrome
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  • combined immunodeficiency
  • combined immunodeficiency disease
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  • combined immunodeficiency disease
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  • combined immunodeficiency syndrome
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  • combined immunodeficiency syndrome
    º¹ÇÕÇü¸é¿ª°áÇÌÁõ(Èıº)
  • common variable immunodeficiency
    Common variable immunodeficiency
  • congenital immunodeficiency syndrome
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  • congenital immunodeficiency syndrome
    ¼±Ãµ¼º¸é¿ª°áÇÌÁõ(Èıº)
  • hiv(human immunodeficiency virus)
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  • huma immunodeficiency virus
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AIDSTRIALS clinical trials of acquired immunodeficiency syndrome drugs [MEDLARS data base]
ARC accelerating rate calorimetry; acquired immunodeficiency syndrome-related complex; active renin conc...
ARV acquired immunodeficiency syndrome-related virus; anterior right ventricle; avian reovirus
ASHAC acquired immunodeficiency syndrome self-help and care
CVI cardiovascular incident; cardiovascular insufficiency; cerebrovascular incident; cerebrovascular ins...
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CID Combined immunodeficiency
CVI Common variable immunodeficiency
FIV Feline Immunodeficiency Virus
AIDS HIV)-acquired immunodeficiency syndrome
HIV-1 Human Immunodeficiency Virus
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ateliotic dwarfism A state in which the secretion of all anterior pituitary hormones is inadequate or absent; caused by a variety of disorders that result in destruction or loss of function of all or most of the anterior pituitary gland. Rare forms of PHP are inherited as autosomal recessive or as an X-linked recessive.
Synonym: ateliotic dwarfism, hypophyseal cachexia, hypophysial cachexia.
(05 Mar 2000)
camptomelic dwarfism Dwarfism with shortening of the lower limbs due to anterior bending of the femur and tibia.
(05 Mar 2000)
panhypopituitary dwarfism Type I is an autosomal recessive disorder with deficient human growth hormone, ACTH, FSH, etc., having delayed sexual development, hypothyroidism, and adrenal insufficiency; type II is similar but is an X-linked disorder.
(05 Mar 2000)
mesomelic dwarfism Dwarfism with shortness of the forearms and lower legs.
(05 Mar 2000)
metatropic dwarfism Congenital disproportionate dwarfism in which the trunk is long relative to the limbs at birth but undergoes reversal of this proportion with subsequent development.
(05 Mar 2000)
chondrodystrophic dwarfism See: chondrodystrophy.
(05 Mar 2000)
Robinow dwarfism Dwarfism associated with foetal face, acral dysostosis, and genital anomalies; there is also an autosomal recessive form.
(05 Mar 2000)
micromelic dwarfism Dwarfism with abnormally short or small limbs.
(05 Mar 2000)
phocomelic dwarfism Dwarfism in which the diaphyses of the long bones are abnormally short or the intermediate parts of the limbs are absent.
(05 Mar 2000)
physiologic dwarfism Dwarfism characterised by normal development that is at a strikingly lesser rate than that for members of the same family, race, or other races.
Synonym: primordial dwarfism, true dwarfism.
(05 Mar 2000)
pituitary dwarfism Short stature due to underpreformance of the pituitary gland (specifically of the anterior pituitary).
(12 Dec 1998)
polydystrophic dwarfism <biochemistry, syndrome> An error of mucopolysaccharide metabolism due to deficiency of the lysosomal enzyme arylsulphatase B.
It is characterised by excretion of dermatan sulfate in the urine, growth retardation, lumbar kyphosis, sternal protrusion, genu valgum, usually hepatosplenomegaly, and no mental retardation.
Onset occurs after two years of age.
Inheritance: autosomal recessive.
Synonym: polydystrophic dwarfism, mucopolysaccharidosis type VI.
(05 Mar 2000)
primordial dwarfism Dwarfism characterised by normal development that is at a strikingly lesser rate than that for members of the same family, race, or other races.
Synonym: primordial dwarfism, true dwarfism.
(05 Mar 2000)
Seckel dwarfism <syndrome> An autosomal recessive disorder characterised by low birth weight, dwarfism, microcephaly, large eyes, beaked nose, receding mandible, and moderate mental retardation.
Synonym: Seckel dwarfism.
(05 Mar 2000)
senile dwarfism Dwarfism characterised by craniofacial anomalies with progeroid appearance.
(05 Mar 2000)
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