congenital myxedema
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Congenital hypothyroidism — Classification and external resources ICD 10 E00, E03.0, E03.1 … Wikipedia
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency — Classification and external resources Deficient 21 Hydroxylase can lead to accumulation of 17 Hydroxyprogesterone ICD … Wikipedia
Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency — Classification and external resources OMIM 202010 eMedicine article/117012 11β Hydroxylase deficient con … Wikipedia
Congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency — Classification and external resources OMIM 202110 DiseasesDB 1841 … Wikipedia
Congenital adrenal hyperplasia due to 3 beta-hydroxysteroid dehydrogenase deficiency — Classification and external resources Cortisol ICD 10 E … Wikipedia
Myxedema — Myxoedema Classification and external resources Hyaluronan, an example of a mucopolysaccharide. ICD 10 E … Wikipedia
Congenital adrenal hyperplasia — CAH redirects here. For other meanings of CAH see CAH (disambiguation) Congenital adrenal hyperplasia Classification and external resources ICD 10 E25.0 ICD 9 … Wikipedia
myxedema — Hypothyroidism characterized by a relatively hard edema of subcutaneous tissue, with increased content of mucins (proteoglycans) in the fluid; characterized by somnolence, slow mentation, dryness and loss of hair, increased fluid in … Medical dictionary
congenitalmyxedema — congenital myxedema n. See cretinism. * * * … Universalium
hypothyroidism — Diminished production of thyroid hormone, leading to clinical manifestations of thyroid insufficiency, including low metabolic rate, tendency to weight gain, somnolence and sometimes myxedema. SYN: athyrea … Medical dictionary