Endocrine, nutritional and metabolic disease stubs
- Abscess of thymus
- Achard–Thiers syndrome
- Adams–Nance syndrome
- Adiposogenital dystrophy
- Adrenalitis
- Adrenocortical hyperfunction
- Adrenocorticotropic hormone deficiency
- Amino acid transport disorder
- Androgen-dependent condition
- Androgen-induced hermaphroditism
- Androgen deprivation-induced senescence
- AREDYLD syndrome
- Chondrodysplasia Blomstrand
- Coenzyme Q10 deficiency
- Congenital disorders of amino acid metabolism
- Cuban neuropathy
- Cystica profunda
- Desmosterolosis
- Dunnigan familial partial lipodystrophy
- Familial dysalbuminemic hyperthyroxinemia
- Fanconi–Bickel syndrome
- Gangliosidosis
- Garrod's tetrad
- Glucocorticoid deficiency 1
- Glycoproteinosis
- Hepatic porphyria
- Hepatoerythropoietic porphyria
- Hereditary hyperbilirubinemia
- Hydrops-ectopic calcification-moth-eaten skeletal dysplasia
- Hyperaminoacidemia
- Hypergonadism
- Hypergonadotropic hypergonadism
- Hyperthyroxinemia
- Idiopathic hypoglycemia
- Inborn errors of purine–pyrimidine metabolism
- Inborn errors of renal tubular transport
- Lathosterolosis
- Leukotriene C4 synthase deficiency
- Molybdenum deficiency
- Multiple carboxylase deficiency
- Palpation thyroiditis
- Parathyroiditis
- Pelvic lipomatosis
- Pentosuria
- Pituitary ACTH hypersecretion
- Polar T3 syndrome
- Psoas muscle abscess
- Subacute thyroiditis
- Succinyl-CoA:3-oxoacid CoA transferase deficiency
- Sulfatidosis
- Template:Endocrine-disease-stub
- Thymic hypoplasia
- Thyrotoxicosis factitia
- Undervirilization
- Uremic frost
- Van Wyk and Grumbach syndrome
- Zeism
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Endocrine, nutritional and metabolic disease stubs
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