Category:Endocrine diseases
From WikiMD.com Medical Encyclopedia
 | This category reflects the organization of International Statistical Classification of Diseases and Related Health Problems, 10th Revision. Generally, diseases outlined within the ICD-10 codes E00-E35 should be included in this category. |
Subcategories
This category has the following 7 subcategories, out of 7 total.
A
E
P
T
Pages in category "Endocrine diseases"
The following 200 pages are in this category, out of 341 total.
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- Achard syndrome
- Achard–Thiers syndrome
- Acute adrenal insufficiency
- Addison’s disease
- Adiposogenital dystrophy
- Adrenal cancer
- Adrenal cortical carcinoma
- Adrenal gland disorder
- Adrenal gland hyperfunction
- Adrenal hypertension
- Adrenal suppression
- Adrenalitis
- Adrenocortical hyperfunction
- Adrenocorticotropic hormone deficiency
- Adrenoleukodystrophy
- Adult-onset diabetes
- Agalactorrhea
- AIS
- Albright like syndrome
- Aldosterone deficiency
- Aldosterone synthase deficiency
- Alpha cell hyperplasia
- Androgen receptor deficiency
- Anovulation
- Apid
- Army Medical Service (Germany)
- Aromatase excess syndrome
- Ateliosis
- Autoimmune adrenalitis
- Autoimmune polyendocrine syndrome
- Autoimmune polyendocrine syndrome type 1
- Autoimmune Polyendocrine Syndrome Type 1
- Autoimmune polyendocrine syndrome type 2
- Autoimmune polyendocrine syndrome type 3
- Autoimmune polyendocrinopathy
- Autoimmune polyglandular syndrome type 1
- Autoimmune polyglandular syndrome type 2
- Autoimmune polyglandular syndrome type 3
- Autosomal dominant hypophosphatemic rickets
C
- Carney syndrome
- Central diabetes insipidus
- Cerebral salt-wasting syndrome
- Complications of diabetes mellitus
- Congenital adrenal hyperplasia
- Congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency
- Congenital adrenal hyperplasia due to 21-hydroxylase deficiency
- Congenital adrenal hyperplasia due to 3 beta-hydroxysteroid dehydrogenase deficiency
- Congenital adrenal hyperplasia due to 3β-hydroxysteroid dehydrogenase deficiency
- Congenital growth hormone deficiency
- Congenital hypothyroidism
- Congenital iodine deficiency syndrome
- Conn syndrome
- Conn's
- Conn's syndrome
- Corticosteroid-induced lipodystrophy
- Crandall syndrome
- Cretic
- Cushing disease
- Cushing's disease
- Cutis verticis gyrata thyroid aplasia mental retardation
- Cystic fibrosis-related diabetes
D
- DAVID syndrome
- Diab
- Diabetes in cats
- Diabetes insipidus
- Diabetes Insipidus
- Diabetes insipidus, nephrogenic type 1
- Diabetes insipidus, nephrogenic type 2
- Diabetes insipidus, nephrogenic type 3
- Diabetes insipidus, nephrogenic, recessive type
- Diabetes
- Diabetes UK
- Differences of sex development
- Distal renal tubular acidosis
- Double diabetes
- Drug-induced lipodystrophy
- Dunnigan familial partial lipodystrophy
- Dyshormonogenesis
E
- Ectodermal dysplasia hypohidrotic hypothyroidism ciliary dyskinesia
- Empty sella syndrome
- Endemic cretinism
- Endemic goitre
- Endocrine bone disease
- Endocrine disease
- Equine metabolic syndrome
- Estrogen insensitivity syndrome
- Eunuchoidism familial
- Euthyroid sick syndrome
- Excess ovarian androgen release syndrome
F
- Familial dysalbuminemic hyperthyroxinemia
- Familial hyperaldosteronism
- Familial hyperaldosteronism type 1
- Familial hyperaldosteronism type 3
- Familial hypocalciuric hypercalcemia
- Familial hypothyroidism
- Familial male-limited precocious puberty
- Familial medullary thyroid cancer
- Familial non-immune hyperthyroidism
- Fertile eunuch syndrome
- Fetal methimazole syndrome
- Fibrocalculous pancreatopathy
- Fröhlich
G
- Galactorrhea hyperprolactinemia
- Genital dwarfism
- Gestational diabetes
- Gestational diabetes mellitus
- Giga
- Glucagonoma
- Glucocorticoid deficiency, familial
- Goiter
- Goitre
- Gonadal dysgenesis
- Gonadal dysgenesis XY type associated anomalies
- Gonadotropin insensitivity
- Granulomatous thyroiditis
- Grave
- Graves
- Grinspan's syndrome
- Gynecomastia
H
- HAIR-AN syndrome
- Hair-an syndrome
- Hashimoto thyroiditis
- Hashimoto's encephalopathy
- Hashimoto's thyroiditis
- Hashitoxicosis
- Hoffmann syndrome
- Hyperaldosteronism
- Hyperaldosteronism familial type 2
- Hypercalcemia, familial benign
- Hypercalcemia, familial benign type 2
- Hyperglycaemia
- Hyperglycemia
- Hypergonadotropic
- Hypergonadotropic hypergonadism
- Hypergonadotropic hypogonadism
- Hyperinsulinemia
- Hyperinsulinism
- Hyperinsulinism in children, congenital
- Hyperinsulinism, focal
- Hyperinsulinism-hyperammonemia syndrome
- Hyperosmolar syndrome
- Hyperostosis frontalis interna
- Hyperparathyroidism
- Hyperparathyroidism, neonatal severe primary
- Hyperpituitarism
- Hypertensive hypokalemia familial
- Hyperthyroxinemia
- Hypoaldosteronism
- Hypocalcaemia
- Hypogonadotropic hypogonadism-anosmia, X linked
- Hypoketonemic hypoglycemia
- Hypoparathyroidism X linked
- Hypophysitis
- Hypoprolactinemia
- Hyporeninemic hypoaldosteronism
- Hypotensive
- Hypothalamic disease
- Hypothalamic hamartoblastoma syndrome
- Hypothyroidism
I
K
L
- Labile diabetes
- Late onset congenital adrenal hyperplasia
- Latent autoimmune diabetes in adults
- Latent diabetes
- LCH
- Leydig cell hypoplasia
- Liddle syndrome
- Lipoatrophic diabetes
- Lipohypertrophy
- List of ICD-9 codes 240–279: endocrine, nutritional and metabolic diseases, and immunity disorders
- Local gigantism
- Luteinizing hormone insensitivity
