Pages that link to "Template:Endocrine-disease-stub"
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- Idiopathic hypoglycemia (transclusion) (links | edit)
- Pelvic lipomatosis (transclusion) (links | edit)
- Hypochloremia (transclusion) (links | edit)
- Calcinosis (transclusion) (links | edit)
- Ateliosis (transclusion) (links | edit)
- Overnutrition (transclusion) (links | edit)
- Gangliosidosis (transclusion) (links | edit)
- Hyperchloremic acidosis (transclusion) (links | edit)
- Glycoproteinosis (transclusion) (links | edit)
- Zeism (transclusion) (links | edit)
- Adams–Nance syndrome (transclusion) (links | edit)
- Glucocorticoid deficiency 1 (transclusion) (links | edit)
- Boron deficiency (medicine) (transclusion) (links | edit)
- Adrenalitis (transclusion) (links | edit)
- AREDYLD syndrome (transclusion) (links | edit)
- Autosomal dominant hypophosphatemic rickets (transclusion) (links | edit)
- Hepatic porphyria (transclusion) (links | edit)
- Lipoatrophic diabetes (transclusion) (links | edit)
- Hepatoerythropoietic porphyria (transclusion) (links | edit)
- Hyperaminoacidemia (transclusion) (links | edit)
- Analbuminaemia (transclusion) (links | edit)
- Hyperproinsulinemia (transclusion) (links | edit)
- Thyroid dyshormonogenesis (transclusion) (links | edit)
- Pentosuria (transclusion) (links | edit)
- Pituicytoma (transclusion) (links | edit)
- Thyrotoxicosis factitia (transclusion) (links | edit)
- Uremic frost (transclusion) (links | edit)
- Fanconi–Bickel syndrome (transclusion) (links | edit)
- Inborn errors of purine–pyrimidine metabolism (transclusion) (links | edit)
- Hereditary hyperbilirubinemia (transclusion) (links | edit)
- Congenital disorders of amino acid metabolism (transclusion) (links | edit)
- Amino acid transport disorder (transclusion) (links | edit)
- Inborn errors of renal tubular transport (transclusion) (links | edit)
- Tyrosinemia type III (transclusion) (links | edit)
- Multiple carboxylase deficiency (transclusion) (links | edit)
- Adrenocortical hyperfunction (transclusion) (links | edit)
- Abscess of thymus (transclusion) (links | edit)
- Sulfatidosis (transclusion) (links | edit)
- Succinyl-CoA:3-oxoacid CoA transferase deficiency (transclusion) (links | edit)
- Hashitoxicosis (transclusion) (links | edit)
- Androgen-dependent condition (transclusion) (links | edit)
- Hyperthyroxinemia (transclusion) (links | edit)
- Familial dysalbuminemic hyperthyroxinemia (transclusion) (links | edit)
- Desmosterolosis (transclusion) (links | edit)
- Lathosterolosis (transclusion) (links | edit)
- Hydrops-ectopic calcification-moth-eaten skeletal dysplasia (transclusion) (links | edit)
- Dunnigan familial partial lipodystrophy (transclusion) (links | edit)
- Thymic hypoplasia (transclusion) (links | edit)
- Parathyroiditis (transclusion) (links | edit)
- MODY 1 (transclusion) (links | edit)