Wikipedia:MeSH C19
From Wikipedia, the free encyclopedia
The following is a list of the "C" codes for MeSH. It is a product of the United States National Library of Medicine.
Source for content is here. (File "2006 MeSH Trees".)
[edit] MeSH C19 --- endocrine system diseases
[edit] MeSH C19.053 --- adrenal gland diseases
[edit] MeSH C19.053.098 --- adrenal cortex diseases
- MeSH C19.053.098.265 --- adrenal cortex neoplasms
- MeSH C19.053.098.265.500 --- adrenocortical adenoma
- MeSH C19.053.098.265.750 --- adrenocortical carcinoma
[edit] MeSH C19.053.347 --- adrenal gland neoplasms
- MeSH C19.053.347.500 --- adrenal cortex neoplasms
- MeSH C19.053.347.500.500 --- adrenocortical adenoma
- MeSH C19.053.347.500.750 --- adrenocortical carcinoma
[edit] MeSH C19.053.440 --- adrenal hyperplasia, congenital
[edit] MeSH C19.053.500 --- adrenal insufficiency
- MeSH C19.053.500.263 --- addison disease
- MeSH C19.053.500.270 --- adrenoleukodystrophy
- MeSH C19.053.500.480 --- hypoaldosteronism
- MeSH C19.053.500.740 --- waterhouse-friderichsen syndrome
[edit] MeSH C19.053.800 --- adrenocortical hyperfunction
- MeSH C19.053.800.367 --- cushing syndrome
- MeSH C19.053.800.604 --- hyperaldosteronism
- MeSH C19.053.800.604.249 --- bartter syndrome
[edit] MeSH C19.246 --- diabetes mellitus
[edit] MeSH C19.246.099 --- diabetes complications
- MeSH C19.246.099.500 --- diabetic angiopathies
- MeSH C19.246.099.500.191 --- diabetic foot
- MeSH C19.246.099.500.382 --- diabetic retinopathy
- MeSH C19.246.099.750 --- diabetic coma
- MeSH C19.246.099.750.490 --- hyperglycemic hyperosmolar nonketotic coma
- MeSH C19.246.099.812 --- diabetic ketoacidosis
- MeSH C19.246.099.875 --- diabetic nephropathies
- MeSH C19.246.099.937 --- diabetic neuropathies
- MeSH C19.246.099.937.250 --- diabetic foot
- MeSH C19.246.099.968 --- fetal macrosomia
[edit] MeSH C19.246.200 --- diabetes, gestational
[edit] MeSH C19.246.240 --- diabetes mellitus, experimental
[edit] MeSH C19.246.267 --- diabetes mellitus, type 1
[edit] MeSH C19.246.300 --- diabetes mellitus, type 2
[edit] MeSH C19.246.774 --- prediabetic state
[edit] MeSH C19.297 --- dwarfism
[edit] MeSH C19.297.155 --- congenital hypothyroidism
[edit] MeSH C19.297.312 --- dwarfism, pituitary
[edit] MeSH C19.297.656 --- laron syndrome
[edit] MeSH C19.344 --- endocrine gland neoplasms
[edit] MeSH C19.344.078 --- adrenal gland neoplasms
- MeSH C19.344.078.265 --- adrenal cortex neoplasms
- MeSH C19.344.078.265.500 --- adrenocortical adenoma
- MeSH C19.344.078.265.750 --- adrenocortical carcinoma
[edit] MeSH C19.344.400 --- multiple endocrine neoplasia
- MeSH C19.344.400.500 --- multiple endocrine neoplasia type 1
- MeSH C19.344.400.505 --- multiple endocrine neoplasia type 2a
- MeSH C19.344.400.510 --- multiple endocrine neoplasia type 2b
[edit] MeSH C19.344.410 --- ovarian neoplasms
- MeSH C19.344.410.398 --- granulosa cell tumor
- MeSH C19.344.410.464 --- luteoma
- MeSH C19.344.410.531 --- meigs syndrome
- MeSH C19.344.410.648 --- sertoli-leydig cell tumor
- MeSH C19.344.410.765 --- thecoma
[edit] MeSH C19.344.421 --- pancreatic neoplasms
- MeSH C19.344.421.249 --- adenoma, islet cell
- MeSH C19.344.421.249.500 --- insulinoma
- MeSH C19.344.421.500 --- carcinoma, islet cell
- MeSH C19.344.421.500.124 --- gastrinoma
- MeSH C19.344.421.500.249 --- glucagonoma
- MeSH C19.344.421.500.500 --- somatostatinoma
- MeSH C19.344.421.500.750 --- vipoma
- MeSH C19.344.421.750 --- carcinoma, pancreatic ductal
[edit] MeSH C19.344.473 --- paraneoplastic endocrine syndromes
[edit] MeSH C19.344.525 --- parathyroid neoplasms
[edit] MeSH C19.344.609 --- pituitary neoplasms
- MeSH C19.344.609.145 --- acth-secreting pituitary adenoma
- MeSH C19.344.609.145.500 --- nelson syndrome
- MeSH C19.344.609.292 --- growth hormone-secreting pituitary adenoma
- MeSH C19.344.609.792 --- prolactinoma
[edit] MeSH C19.344.762 --- testicular neoplasms
[edit] MeSH C19.344.894 --- thyroid neoplasms
[edit] MeSH C19.391 --- gonadal disorders
[edit] MeSH C19.391.482 --- hypogonadism
- MeSH C19.391.482.293 --- eunuchism
- MeSH C19.391.482.600 --- kallmann syndrome
- MeSH C19.391.482.629 --- klinefelter syndrome
- MeSH C19.391.482.814 --- sexual infantilism
[edit] MeSH C19.391.630 --- ovarian diseases
- MeSH C19.391.630.050 --- anovulation
- MeSH C19.391.630.450 --- oophoritis
- MeSH C19.391.630.580 --- ovarian cysts
- MeSH C19.391.630.580.765 --- polycystic ovary syndrome
- MeSH C19.391.630.611 --- ovarian failure, premature
- MeSH C19.391.630.642 --- ovarian hyperstimulation syndrome
- MeSH C19.391.630.705 --- ovarian neoplasms
- MeSH C19.391.630.705.265 --- brenner tumor
- MeSH C19.391.630.705.331 --- carcinoma, endometrioid
- MeSH C19.391.630.705.398 --- granulosa cell tumor
- MeSH C19.391.630.705.464 --- luteoma
- MeSH C19.391.630.705.531 --- meigs syndrome
- MeSH C19.391.630.705.648 --- sertoli-leydig cell tumor
- MeSH C19.391.630.705.765 --- thecoma
[edit] MeSH C19.391.690 --- puberty, delayed
[edit] MeSH C19.391.693 --- puberty, precocious
[edit] MeSH C19.391.775 --- sex differentiation disorders
- MeSH C19.391.775.129 --- adrenogenital syndrome
- MeSH C19.391.775.260 --- freemartinism
- MeSH C19.391.775.309 --- gonadal dysgenesis
- MeSH C19.391.775.309.193 --- gonadal dysgenesis, 46,xx
- MeSH C19.391.775.309.388 --- gonadal dysgenesis, 46,xy
- MeSH C19.391.775.309.391 --- gonadal dysgenesis, mixed
- MeSH C19.391.775.309.872 --- turner syndrome
- MeSH C19.391.775.316 --- hermaphroditism
- MeSH C19.391.775.316.313 --- hermaphroditism, true
- MeSH C19.391.775.316.627 --- pseudohermaphroditism
- MeSH C19.391.775.316.627.500 --- androgen-insensitivity syndrome
- MeSH C19.391.775.370 --- hyperandrogenism
- MeSH C19.391.775.425 --- kallmann syndrome
- MeSH C19.391.775.454 --- klinefelter syndrome
[edit] MeSH C19.391.829 --- testicular diseases
- MeSH C19.391.829.258 --- cryptorchidism
- MeSH C19.391.829.493 --- orchitis
- MeSH C19.391.829.782 --- testicular neoplasms
- MeSH C19.391.829.782.500 --- sertoli-leydig cell tumor
[edit] MeSH C19.642 --- parathyroid diseases
[edit] MeSH C19.642.355 --- hyperparathyroidism
- MeSH C19.642.355.239 --- hyperparathyroidism, primary
- MeSH C19.642.355.480 --- hyperparathyroidism, secondary
- MeSH C19.642.355.480.500 --- renal osteodystrophy
[edit] MeSH C19.642.482 --- hypoparathyroidism
[edit] MeSH C19.642.713 --- parathyroid neoplasms
[edit] MeSH C19.700 --- pituitary diseases
[edit] MeSH C19.700.159 --- diabetes insipidus
- MeSH C19.700.159.750 --- diabetes insipidus, neurogenic
- MeSH C19.700.159.875 --- wolfram syndrome
[edit] MeSH C19.700.320 --- empty sella syndrome
[edit] MeSH C19.700.355 --- hyperpituitarism
- MeSH C19.700.355.179 --- acromegaly
- MeSH C19.700.355.528 --- gigantism
- MeSH C19.700.355.600 --- hyperprolactinemia
- MeSH C19.700.355.800 --- pituitary acth hypersecretion
[edit] MeSH C19.700.482 --- hypopituitarism
[edit] MeSH C19.700.490 --- inappropriate adh syndrome
[edit] MeSH C19.700.725 --- pituitary apoplexy
[edit] MeSH C19.700.734 --- pituitary neoplasms
- MeSH C19.700.734.145 --- acth-secreting pituitary adenoma
- MeSH C19.700.734.145.500 --- nelson syndrome
- MeSH C19.700.734.292 --- growth hormone-secreting pituitary adenoma
- MeSH C19.700.734.792 --- prolactinoma
[edit] MeSH C19.787 --- polyendocrinopathies, autoimmune
[edit] MeSH C19.874 --- thyroid diseases
[edit] MeSH C19.874.255 --- euthyroid sick syndromes
[edit] MeSH C19.874.283 --- goiter
- MeSH C19.874.283.300 --- goiter, endemic
- MeSH C19.874.283.501 --- goiter, nodular
- MeSH C19.874.283.601 --- goiter, substernal
- MeSH C19.874.283.605 --- graves disease
- MeSH C19.874.283.605.500 --- graves ophthalmopathy
- MeSH C19.874.283.802 --- lingual goiter
[edit] MeSH C19.874.397 --- hyperthyroidism
- MeSH C19.874.397.370 --- graves disease
- MeSH C19.874.397.370.500 --- graves ophthalmopathy
- MeSH C19.874.397.685 --- thyrotoxicosis
- MeSH C19.874.397.685.905 --- thyroid crisis
[edit] MeSH C19.874.410 --- hyperthyroxinemia
- MeSH C19.874.410.249 --- hyperthyroxinemia, familial dysalbuminemic
- MeSH C19.874.410.500 --- thyroid hormone resistance syndrome
[edit] MeSH C19.874.482 --- hypothyroidism
[edit] MeSH C19.874.689 --- thyroid dysgenesis
- MeSH C19.874.689.500 --- lingual thyroid
- MeSH C19.874.689.500.500 --- lingual goiter
[edit] MeSH C19.874.788 --- thyroid neoplasms
[edit] MeSH C19.874.871 --- thyroiditis
- MeSH C19.874.871.102 --- thyroiditis, autoimmune
- MeSH C19.874.871.102.500 --- hashimoto disease
- MeSH C19.874.871.102.750 --- postpartum thyroiditis
- MeSH C19.874.871.900 --- thyroiditis, subacute
- MeSH C19.874.871.910 --- thyroiditis, suppurative
[edit] MeSH C19.874.902 --- thyrotoxicosis
- MeSH C19.874.902.905 --- thyroid crisis