This article needs to be updated. The reason given is: no files for 2006 are listed at the cited source, but files for 2013 are there; NLM releases this information annually.(February 2020) |
The following is a partial list of the "C" codes for Medical Subject Headings (MeSH), as defined by the United States National Library of Medicine (NLM).
This list continues the information at List of MeSH codes (C18). Codes following these are found at List of MeSH codes (C20). For other MeSH codes, see List of MeSH codes.
The source for this content is the set of 2006 MeSH Trees from the NLM.
MeSH C19 – endocrine system diseases edit
MeSH C19.053 – adrenal gland diseases edit
MeSH C19.053.098 – adrenal cortex diseases edit
- MeSH C19.053.098.265 – adrenal cortex neoplasms
- MeSH C19.053.098.265.500 – adrenocortical adenoma
- MeSH C19.053.098.265.750 – adrenocortical carcinoma
MeSH C19.053.347 – adrenal gland neoplasms edit
- MeSH C19.053.347.500 – adrenal cortex neoplasms
- MeSH C19.053.347.500.500 – adrenocortical adenoma
- MeSH C19.053.347.500.750 – adrenocortical carcinoma
MeSH C19.053.440 – adrenal hyperplasia, congenital edit
MeSH C19.053.500 – adrenal insufficiency edit
- 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
MeSH C19.053.800 – adrenocortical hyperfunction edit
- MeSH C19.053.800.367 – cushing syndrome
- MeSH C19.053.800.604 – hyperaldosteronism
- MeSH C19.053.800.604.249 – bartter syndrome
MeSH C19.246 – diabetes mellitus edit
MeSH C19.246.099 – diabetes complications edit
- 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
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 edit
- MeSH C19.344.078.265 – adrenal cortex neoplasms
- MeSH C19.344.078.265.500 – adrenocortical adenoma
- MeSH C19.344.078.265.750 – adrenocortical carcinoma
MeSH C19.344.400 – multiple endocrine neoplasia edit
- 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
MeSH C19.344.410 – ovarian neoplasms edit
- 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
MeSH C19.344.421 – pancreatic neoplasms edit
- 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
MeSH C19.344.473 – paraneoplastic endocrine syndromes edit
MeSH C19.344.525 – parathyroid neoplasms edit
MeSH C19.344.609 – pituitary neoplasms edit
- 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
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 edit
- 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
MeSH C19.391.630 – ovarian diseases edit
- 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
MeSH C19.391.690 – puberty, delayed edit
MeSH C19.391.693 – puberty, precocious edit
MeSH C19.391.775 – sex differentiation disorders edit
- 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
MeSH C19.391.829 – testicular diseases edit
- 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
MeSH C19.642 – parathyroid diseases edit
MeSH C19.642.355 – hyperparathyroidism edit
- MeSH C19.642.355.239 – hyperparathyroidism, primary
- MeSH C19.642.355.480 – hyperparathyroidism, secondary
- MeSH C19.642.355.480.500 – renal osteodystrophy
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 edit
MeSH C19.700.320 – empty sella syndrome edit
MeSH C19.700.355 – hyperpituitarism edit
- 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
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 edit
- 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
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 edit
- 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
MeSH C19.874.397 – hyperthyroidism edit
- 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
MeSH C19.874.410 – hyperthyroxinemia edit
- MeSH C19.874.410.249 – hyperthyroxinemia, familial dysalbuminemic
- MeSH C19.874.410.500 – thyroid hormone resistance syndrome
MeSH C19.874.482 – hypothyroidism edit
MeSH C19.874.689 – thyroid dysgenesis edit
MeSH C19.874.788 – thyroid neoplasms edit
MeSH C19.874.871 – thyroiditis edit
- 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
MeSH C19.874.902 – thyrotoxicosis edit
MeSH C19.927 – tuberculosis, endocrine edit
The list continues at List of MeSH codes (C20).