Condition library · 101 conditions
Endocrinology conditions
Hormone and gland conditions — thyroid, adrenal, pituitary and others.
Doctors for these conditions are listed as endocrinologists.
All endocrinology conditions
A
- Acquired generalized lipodystrophy
- Acromegaly
- Acute adrenal insufficiency
- Addison Disease
- Adenohypophysitis
- Arginine vasopressin deficiency
- Aromatase deficiency
- Aromatase excess syndrome
- Autoimmune Addison disease
- Autoimmune hypoparathyroidism
- Autoimmune polyendocrinopathy type 3
- Autoimmune polyendocrinopathy type 4
- Autosomal dominant hypocalcemia
- Autosomal semi-dominant severe lipodystrophic laminopathy
C
- Carney complex
- Cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome
- Combined pituitary hormone deficiencies, genetic forms
- Combined pituitary hormone deficiency
- Complete LCAT deficiency
- Congenital generalized lipodystrophy
- Congenital hypothyroidism
- Congenital hypothyroidism due to maternal intake of antithyroid drugs
- Corticosteroid-binding globulin deficiency
- Craniopharyngioma
- Cushing disease
- Cushing syndrome due to bilateral macronodular adrenocortical disease
- Cushing syndrome due to ectopic ACTH secretion
- Cushing's Syndrome
D
E
F
- Familial glucocorticoid deficiency
- Familial isolated hyperparathyroidism
- Familial isolated pituitary adenoma
- Familial lipoprotein lipase deficiency
- Familial partial lipodystrophy, Dunnigan type
- Familial thyroid dyshormonogenesis
- Fish-eye disease
- Fragile X-associated primary ovarian insufficiency
- Functioning gonadotropic adenoma
G
H
I
K
L
M
N
O
P
- Pancreatic hypoplasia-diabetes-congenital heart disease syndrome
- Panhypophysitis
- Pediatric-onset Graves disease
- Pheochromocytoma
- Pituitary apoplexy
- Pituitary dermoid and epidermoid cysts
- Pituitary Tumors
- Polycystic Ovary Syndrome
- Polyendocrine-polyneuropathy syndrome
- PPARG-related familial partial lipodystrophy
- PPoma
- Primary hypergonadotropic hypogonadism-partial alopecia syndrome
- Pseudohypoparathyroidism type 1A
- Pseudohypoparathyroidism type 1B
- Pseudohypoparathyroidism type 1C