E00-E90. Diseases of the endocrine system, nutritional and metabolic diseases: clinical guidelines
ICD-10 Class IV — 72 guidelines of the Russian Ministry of Health across 49 categories.
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- X-linked adrenoleukodystrophy
- Amenorrhea and oligomenorrhea
- Amiodarone-induced thyroid dysfunction
- Maple syrup urine disease
- Gaucher disease
- Niemann-Pick disease type C
- Pompe disease
- Fabry disease
- Congenital adrenal hyperplasia (adrenogenital syndrome)
- Congenital adrenal hyperplasia (adrenogenital syndrome)
- Congenital hyperinsulinism
- Congenital hypothyroidism in children
- Hypoparathyroidism in adults
- Hypopituitarism
- Hypothyroidism
- Glutaric aciduria type 1
- 3-Hydroxy-3-methylglutaryl-CoA lyase deficiency
- Diffuse toxic goiter (Graves' disease)
- Other disorders of branched-chain amino acid metabolism (Methylmalonic acidemia/aciduria)
- Other lipid storage disorders (Lysosomal acid lipase deficiency)
- Other sphingolipidoses (Gaucher disease)
- Other sphingolipidoses (Niemann-Pick disease types A, B, A/B)
- Iron deficiency anemia
- Diseases and conditions related to iodine deficiency
- Idiopathic short stature in children and adolescents
- Isovaleric acidemia/aciduria
- Cystic fibrosis
- Classical phenylketonuria and other hyperphenylalaninemias
- Critical lower limb ischemia (CLLI)
- Multiple carboxylase deficiency (Biotinidase and holocarboxylase synthetase deficiencies)
- Urolithiasis
- Mucopolysaccharidosis type I
- Mucopolysaccharidosis type I
- Mucopolysaccharidosis type II
- Mucopolysaccharidosis type II
- Mucopolysaccharidosis type VI
- Mucopolysaccharidosis type VI
- Disorders of sulfur-bearing amino acid metabolism (Homocystinuria)
- Phosphorus metabolism disorders (Hypophosphatasia)
- Disorders of lipoprotein metabolism and other lipidemias
- Disorders of mitochondrial fatty acid $\beta$-oxidation
- Galactose metabolism disorders (Galactosemia)
- Copper metabolism disorders (Wilson disease)
- Hereditary tyrosinemia type 1
- 3-Methylcrotonyl-CoA carboxylase deficiency (3-methylcrotonylglycinuria, methylcrotonyl-CoA carboxylase deficiency)
- Vitamin D deficiency. Rickets.
- Mitochondrial acetoacetyl-CoA thiolase deficiency ($\beta$-ketothiolase deficiency, T2 deficiency)
- Malnutrition in elderly and senile patients
- Malnutrition in children older than 1 year (Protein-energy malnutrition)
- Obesity
- Obesity in children
- Acute and chronic thyroiditis (excluding autoimmune and amiodarone-induced thyroiditis)
- Acute porphyrias
- Primary adrenal insufficiency
- Primary chronic adrenal insufficiency
- Primary hyperparathyroidism
- Precocious puberty
- Propionic acidemia/aciduria
- Type 1 diabetes mellitus in adults
- Type 1 diabetes mellitus in children
- Type 2 diabetes mellitus in adults
- Type 2 diabetes mellitus in children
- Diabetes mellitus: diabetic retinopathy, diabetic macular edema
- Familial Mediterranean fever (Hereditary familial amyloidosis)
- Polycystic ovary syndrome
- Thyroiditis in children
- Thyrotoxicosis with diffuse goiter (Graves' disease), nodular/multinodular goiter
- Toxic and metabolic disorders of the nervous system
- Lung transplantation, heart-lung transplantation, presence of transplanted lung, presence of transplanted heart-lung complex, graft failure and rejection of lung transplant, graft failure and rejection of heart-lung transplant
- Transthyretin familial amyloid polyneuropathy
- Chronic kidney disease (CKD)
- Chronic lower extremity ischemia with symptoms of intermittent claudication (IC)
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