Jump to content

List of MeSH codes (C19)

From Wikipedia, the free encyclopedia

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. Please help update this article to reflect recent events or newly available information. (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

MeSH C19.053 – adrenal gland diseases

MeSH C19.053.098 – adrenal cortex diseases

MeSH C19.053.347 – adrenal gland neoplasms

MeSH C19.053.440 – adrenal hyperplasia, congenital

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

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

MeSH C19.246 – diabetes mellitus

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

MeSH C19.246.200 – diabetes, gestational

MeSH C19.246.240 – diabetes mellitus, experimental

MeSH C19.246.267 – diabetes mellitus, type 1

MeSH C19.246.267.960 – wolfram syndrome

MeSH C19.246.300 – diabetes mellitus, type 2

MeSH C19.246.300.500 – diabetes mellitus, lipoatrophic

MeSH C19.246.774 – prediabetic state

MeSH C19.297 – dwarfism

MeSH C19.297.155 – congenital hypothyroidism

MeSH C19.297.312 – dwarfism, pituitary

MeSH C19.297.656 – laron syndrome

MeSH C19.344 – endocrine gland neoplasms

MeSH C19.344.078 – adrenal gland neoplasms

MeSH C19.344.400 – multiple endocrine neoplasia

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

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

MeSH C19.344.473 – paraneoplastic endocrine syndromes

MeSH C19.344.525 – parathyroid neoplasms

MeSH C19.344.609 – pituitary neoplasms

MeSH C19.344.762 – testicular neoplasms

MeSH C19.344.762.500 – sertoli-leydig cell tumor

MeSH C19.344.894 – thyroid neoplasms

MeSH C19.344.894.800 – thyroid nodule

MeSH C19.391 – gonadal disorders

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

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

MeSH C19.391.690 – puberty, delayed

MeSH C19.391.693 – puberty, precocious

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

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

MeSH C19.642 – parathyroid diseases

MeSH C19.642.355 – hyperparathyroidism

MeSH C19.642.482 – hypoparathyroidism

MeSH C19.642.482.500 – digeorge syndrome

MeSH C19.642.713 – parathyroid neoplasms

MeSH C19.700 – pituitary diseases

MeSH C19.700.159 – diabetes insipidus

MeSH C19.700.320 – empty sella syndrome

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

MeSH C19.700.482 – hypopituitarism

MeSH C19.700.482.311 – dwarfism, pituitary

MeSH C19.700.490 – inappropriate adh syndrome

MeSH C19.700.725 – pituitary apoplexy

MeSH C19.700.734 – pituitary neoplasms

MeSH C19.787 – polyendocrinopathies, autoimmune

MeSH C19.874 – thyroid diseases

MeSH C19.874.255 – euthyroid sick syndromes

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

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

MeSH C19.874.410 – hyperthyroxinemia

MeSH C19.874.482 – hypothyroidism

MeSH C19.874.482.281 – congenital hypothyroidism
MeSH C19.874.482.638 – myxedema

MeSH C19.874.689 – thyroid dysgenesis

MeSH C19.874.689.500 – lingual thyroid
MeSH C19.874.689.500.500 – lingual goiter

MeSH C19.874.788 – thyroid neoplasms

MeSH C19.874.788.800 – thyroid nodule

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

MeSH C19.874.902 – thyrotoxicosis

MeSH C19.874.902.905 – thyroid crisis

MeSH C19.927 – tuberculosis, endocrine

The list continues at List of MeSH codes (C20).

Lists of MeSH codes

Retrieved from "https://en.wikipedia.org/w/index.php?title=List_of_MeSH_codes_(C19)&oldid=1205424116"

Medical Subject Headings

Hidden categories: