Category:Endocrine disorders
From WikiMD's Wellness Encyclopedia
This is a category page. It lists all of the pages in category "Endocrine disorders" as well as all subcategories of category "Endocrine disorders" if any exist.
Pages in category "Endocrine disorders"
The following 186 pages are in this category, out of 186 total.
1
A
B
C
- Cardiomyopathy hypogonadism metabolic anomalies
- Carney complex
- Chondrodysplasia pseudohermaphrodism syndrome
- Clitoromegaly
- Collins–Sakati syndrome
- Congenital adrenal hypoplasia
- Congenital hypogonadotropic hypogonadism
- Cortisol ulcer
- Cortisone reductase deficiency
- Culler–Jones syndrome
- Cushing
- Cushingoid
E
F
G
H
- Hashimoto disease
- Hashimoto’s disease
- Hi-wa itck
- Hormone antagonists
- Hyperandrogenism
- Hypercalcaemia
- Hypercalcemia
- Hypercortisolemia
- Hyperdynamic circulation
- Hyperestrogenism
- Hyperglycerolemia
- Hypergonadism
- Hyperinsulinemic hypoglycemia
- Hyperinsulinism
- Hypermetabolism
- Hyperphosphatemia
- Hyperproinsulinemia
- Hyperprolactinemia
- Hyperprolactinemic SAHA syndrome
- Hyperthecosis
- Hypoadrenalism
- Hypoadrenia
- Hypoandrogenism
- Hypocalcemia
- Hypoestrogenism
- Hypogalactia
- Hypoglycaemia
- Hypoglycemic
- Hypogonadism
- Hypogonadism retinitis pigmentosa
- Hypogonadotropic hypogonadism syndactyly
- Hypothalamic hamartoma
- Hypothyroidism due to iodide transport defect
- Höhn
I
M
- Male lactation
- Male pseudohermaphroditism due to defective LH molecule
- Malouf syndrome
- Mental deficiency-epilepsy-endocrine disorders
- Mental retardation myopathy short stature endocrine defect
- Metabolic syndrome x
- Microcephaly hypergonadotropic hypogonadism short stature
- Microcephaly micropenis convulsions
- MODY 1
- MODY 2
- MODY 6
- MORM syndrome
- Muscular atrophy-ataxia-retinitis pigmentosa-diabetes mellitus syndrome
- Muscular dystrophy congenital infantile cataract hypogonadism
- Myxoma-spotty pigmentation-endocrine overactivity
- Möbius axonal neuropathy hypogonadism
O
P
- Pacak–Zhuang syndrome
- Pcos
- Persistent adrenarche syndrome
- Persistent thyroglossal duct
- Pickardt syndrome
- Pituitary dwarfism
- Pituitary pars intermedia dysfunction
- Polar T3 syndrome
- Polycystic
- Polycystic ovary disease
- Polycystic ovary syndrome
- Polyphagia
- Prader-Willi syndrome
- Prepubertal hypertrichosis
- Primary aldosteronism
- Primary amenorrhea
- Primary ovarian insufficiency
- Progesterone deficiency
- Progestin-induced virilization
- Pseudo-Cushing's syndrome
- Pseudohermaphroditism
- Pseudohermaphroditism female skeletal anomalies
- Pseudohermaphroditism male with gynecomastia
- Pubertal gynecomastia
