Category:Endocrine diseases
From WikiMD's Wellness 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. |
Pages in category "Endocrine diseases"
The following 200 pages are in this category, out of 371 total.
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- Acanthosis nigricans-muscle cramps-acral enlargement syndrome
- Achard syndrome
- Achard-Thiers syndrome
- Achard–Thiers syndrome
- Acropachy
- Acute adrenal insufficiency
- Addison's syndrome
- Addison’s disease
- Adiposogenital dystrophy
- Adrenal cortical carcinoma
- Adrenal gland disorder
- Adrenal gland hyperfunction
- Adrenal haemorrhage
- Adrenal hyperplasia
- Adrenal hypertension
- Adrenal hypoplasia congenita
- Adrenal mass
- Adrenal suppression
- Adrenalism
- Adrenalitis
- Adrenocortical hyperfunction
- Adrenocorticotropic hormone deficiency
- Adult-onset diabetes
- AIS
- Albright like syndrome
- Aldosterone deficiency
- Aldosterone synthase deficiency
- Alpha cell hyperplasia
- Amiodarone induced thyrotoxicosis
- Anovulation
- Ascher
- 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
B
C
- Carney's
- Central diabetes insipidus
- Cerebral salt-wasting syndrome
- Complications of diabetes mellitus
- Congenital adrenal hyperplasia
- 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 craniosynostosis maternal hyperthyroiditis
- Congenital growth hormone deficiency
- Congenital hypothyroidism
- Congenital iodine deficiency syndrome
- Conn's
- Conn's syndrome
- Corticosteroid-induced lipodystrophy
- Crandall syndrome
- Cretic
- Cretinism
- Cushing's disease
- Cutis gyratum acanthosis nigricans craniosynostosis
- Cutis verticis gyrata thyroid aplasia mental retardation
- Cystic fibrosis-related diabetes
D
- DAVID syndrome
- Derbyshire neck
- Diab
- Diabetes in cats
- Diabetes insipidus
- Diabetes Insipidus
- Diabetes
- Diabetic coma
- Diabetic stiff hand syndrome
- Diarrhea polyendocrinopathy infections X linked
- Distal renal tubular acidosis
- Doege–Potter syndrome
- Donohue
- Double diabetes
- Drug-induced lipodystrophy
- Dunnigan
- Dunnigan familial partial lipodystrophy
- Dyshormonogenesis
E
F
G
- Galactorrhea hyperprolactinemia
- Generalized glucocorticoid resistance
- Genital dwarfism
- Gestational diabetes
- Gestational diabetes mellitus
- Gigantism advanced bone age hoarse cry
- Glucagonoma
- GnRH insensitivity
- Goiter
- Goiterogen
- Goitre
- Gonadal dysgenesis XY type associated anomalies
- Gonadotropin insensitivity
- Granulomatous thyroiditis
- Grave
- Graves
- Grinspan's syndrome
- Gynecomastia
H
- HAIR-AN syndrome
- Hashimoto thyroiditis
- Hashimoto's
- Hashimoto's encephalopathy
- Hashimoto's thyroiditis
- Hashitoxicosis
- Hassall's corpuscle
- Hoffmann syndrome
- Hyperadrenalism
- Hyperadrenocorticism
- Hyperaldosteronism
- Hypercalcemia, familial benign
- Hypercalcemia, familial benign type 1
- Hypercalcemia, familial benign type 2
- Hyperglycaemia
- Hyperglycemia
- Hyperglycemic hyperosmolar coma
- Hypergonadotropic
- Hypergonadotropic hypergonadism
- Hypergonadotropic hypogonadism
- Hyperinsulinemia
- Hyperinsulinism due to glutamodehydrogenase deficiency
- Hyperinsulinism-hyperammonemia syndrome
- Hyperosmolar hyperglycemic state
- Hyperosmolar syndrome
- Hyperostosis frontalis interna
- Hyperparathyroidism
- Hyperparathyroidism, neonatal severe primary
- Hyperpituitarism
- Hypertensive hypokalemia familial
- Hyperthyroidism due to mutations in TSH receptor
- Hyperthyroxinemia
- Hypoadrenocorticism
- Hypoaldosteronism
- Hypoathroid
- Hypocalcaemia
- Hypocalciuric hypercalcemia, familial
- Hypogonadotropic hypogonadism-anosmia
- Hypogonadotropic hypogonadism-anosmia, X linked
- Hypoketonemic hypoglycemia
- Hypoparathyroidism X linked
- Hypophysitis
- Hypopituitarism postaxial polydactyly
- Hypoprolactinemia
- Hypotensive
- Hypothalamic disease
- Hypothalamic hamartoblastoma syndrome
- Hypothyroidism
