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hypothyroidism-large muscle syndrome

См. также в других словарях:

  • Kocher-Debre-Semelaigne syndrome — The Kocher Debré Semelaigne syndrome is a (myopathy) of hypothyroidism in infancy or childhood characterised by lower extremity or generalized muscular hypertrophy, myxoedema, short stature and cretinism. The absence of painful spasms and… …   Wikipedia

  • syndrome — The aggregate of symptoms and signs associated with any morbid process, and constituting together the picture of the disease. SEE ALSO: disease. [G. s., a running together, tumultuous concourse; (in med.) a concurrence of symptoms, fr. syn,… …   Medical dictionary

  • muscle disease — ▪ pathology Introduction       any of the diseases and disorders that affect the human muscle system (muscle system, human). Diseases and disorders that result from direct abnormalities of the muscles are called primary muscle diseases; those… …   Universalium

  • Congenital hypothyroidism — Classification and external resources ICD 10 E00, E03.0, E03.1 …   Wikipedia

  • Chronic fatigue syndrome — This article is about the medical condition Chronic fatigue syndrome. For the symptom chronic fatigue, see Fatigue (medical). Chronic fatigue syndrome Classification and external resources ICD 10 G93.3 ICD 9 …   Wikipedia

  • Carpal tunnel syndrome — Classification and external resources Transverse section at the wrist. The median nerve is colored yellow. The carpal tunnel consists of the bones and flexor retinaculum. ICD 1 …   Wikipedia

  • Down syndrome — Classification and external resources Boy with Down syndrome assembling a …   Wikipedia

  • 1p36 deletion syndrome — Classification and external resources A toddler showing facial symptoms of the syndrome. OMIM 607872 DiseasesDB …   Wikipedia

  • Mild androgen insensitivity syndrome — Classification and external resources AIS results when the function of the androgen receptor (AR) is impaired. The AR protein (pictured) mediates the effects of androgens in the human body. ICD 10 E …   Wikipedia

  • Chromosome 1, 1p36 deletion syndrome — Infobox Disease Name = PAGENAME Caption = DiseasesDB = 34535 ICD10 = ICD9 = ICDO = OMIM = 607872 MedlinePlus = eMedicineSubj = eMedicineTopic = eMedicine mult = MeshID = Chromosome 1, 1p36 deletion syndrome is a medical condition caused by a rare …   Wikipedia

  • Cushing's syndrome — Classification and external resources ICD 10 E24 ICD 9 255.0 …   Wikipedia

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