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All Endocrine, Nutritional and Metabolic Diseases

Conditions of the hormone-producing glands, of nutrition, and of the body's chemical processing of food, following ICD-10 Chapter IV (Endocrine, Nutritional and Metabolic Diseases). Belongs here: a hormonal disorder such as a thyroid or pancreatic condition, a deficiency disease caused by inadequate nutrient intake, and an inherited or acquired disorder of metabolism. Does not belong here: a disorder of growth or development that is chromosomal or structurally congenital in origin, grouped under congenital malformations and chromosomal abnormalities.

Facts

Comparison

ICD-10 Chapter Number

IV 1

ICD-10 Code Range

E00-E90 1

All Endocrine, Nutritional and Metabolic Diseases

259 entries

Discoverer

Era (First Described)

Treated By

Body System

ICD-10 Chapter

Communicable or Non-communicable

Transmission Route

1. ICD-10 (Wikipedia)

ICD-10 chapter table, Chapter IV, chapter number
IV | E00-E90 | "Endocrine, nutritional and metabolic diseases"
ICD-10 chapter table, Chapter IV, code range
IV | E00-E90 | "Endocrine, nutritional and metabolic diseases"

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Glutaric acidemia type 2

Glutaric aciduria type 1

Glycogen storage disease type 0

Glycogen storage disease type I

Glycogen storage disease type II

Glycogen storage disease type III

Glycogen storage disease type IV

Glycogen storage disease type V

Glycogen storage disease type VI

Glycogenic hepatopathy

Goiter

Gonadotropin-Releasing Hormone Insensitivity

GRACILE syndrome

Graves' Disease

Growth hormone deficiency

Gunther disease

Haemochromatosis type 3

Hartnup disease

Hashimoto's Thyroiditis

Hemochromatosis type 4

Hereditary coproporphyria

Hereditary fructose intolerance

Hereditary Hemochromatosis

Hereditary hyperbilirubinemia

Hermansky-Pudlak syndrome

Hoffmann syndrome

Homocystinuria

Hunter syndrome

Hutchinson-Gilford Progeria Syndrome

Hyaluronidase deficiency

Hyperaldosteronism

Hyperammonemia

Hyperinsulinemic hypoglycemia

Hyperkalemia

Hyperlysinemia

Hyperosmolar syndrome

Hyperparathyroidism

Hyperphenylalaninemia

Hyperprolactinaemia

Hyperprolactinemia

Hyperprolactinemic SAHA syndrome

Hyperthyroidism

Hypoglycemia

Hyponatremia

Hypoparathyroidism

Hypophosphatasia

Hypopituitarism

Hypothyroidism

Idiopathic Short Stature

Inclusion-cell disease

Isolated 17,20-lyase deficiency

Isovaleric acidemia

Kufs disease

Kwashiorkor

Laron syndrome

Lecithin cholesterol acyltransferase deficiency

Lesch-Nyhan syndrome

Leydig cell hypoplasia

Liddle's syndrome

Lipoatrophy

Lipodystrophy

Lysinuric protein intolerance

Lysosomal storage disease

Malnutrition-inflammation complex

Mannosidosis

Maple Syrup Urine Disease

Marasmus

Maroteaux-Lamy syndrome

McArdle Disease

MDP syndrome

Medium-chain acyl-coenzyme A dehydrogenase deficiency

Megavitamin-B6 syndrome

Menkes disease

MEPAN syndrome

Mercaptolactate-cysteine disulfiduria

Metabolic Syndrome

Methylmalonic acidemias

Methylmalonyl-CoA mutase deficiency

Mevalonate kinase deficiency

Micronutrient deficiency