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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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17β-Hydroxysteroid dehydrogenase III deficiency

3-Methylglutaconic aciduria

5-alpha-Reductase 2 deficiency

6-Pyruvoyltetrahydropterin synthase deficiency

Abetalipoproteinemia

Abnormal basal metabolic rate

Acatalasia

Aceruloplasminemia

Acrodermatitis enteropathica

Acromegaly

Acute intermittent porphyria

Addison's Disease

Adenine phosphoribosyltransferase deficiency

Adenylosuccinate lyase deficiency

Adrenocorticotropic hormone deficiency

Adrenoleukodystrophy

Adult polyglucosan body disease

Albright's hereditary osteodystrophy

Alcohol intolerance

Alexander disease

ALG1-CDG

Alkaptonuria

Alpha-1 Antitrypsin Deficiency

Alpha-mannosidosis

Amyloidosis

Androgen Deficiency

Apparent mineralocorticoid excess syndrome

Argininemia

Argininosuccinic aciduria

Aromatase deficiency

Aromatase excess syndrome

Aspartylglucosaminuria

Autoimmune polyendocrine syndrome type 1

Autoimmune Polyendocrine Syndrome Type 2

Autoimmune polyendocrine syndrome type 3

Autosomal dominant GTP cyclohydrolase I deficiency

Bannayan-Riley-Ruvalcaba syndrome

Bartter syndrome

Batten disease

Beriberi

Beta-ketothiolase deficiency

Branched-chain keto acid dehydrogenase kinase deficiency

Butyrylcholinesterase deficiency

Calcinosis

Carbamoyl phosphate synthetase I deficiency

Carnitine palmitoyltransferase II deficiency

Central diabetes insipidus

Cerebral salt-wasting syndrome

Cerebrotendinous xanthomatosis

Chiari-Frommel Syndrome

Chylomicron retention disease

Citrullinemia

Combined malonic and methylmalonic aciduria

Congenital adrenal hyperplasia

Congenital chloride diarrhea

Congenital generalized lipodystrophy

Copper Deficiency

Crigler-Najjar syndrome

Crystallopathy

Cushing's disease

Cushing's Syndrome

Cystinosis

Cytochrome P450 oxidoreductase deficiency

Danon disease

Deficiency (medicine)

Dehydration

Diabetes Insipidus

Diabetes Mellitus

Diabetic Foot Ulcer

Dihydropyrimidine dehydrogenase deficiency

Donohue syndrome

Dubin-Johnson syndrome

Dunnigan familial partial lipodystrophy

Empty sella syndrome

Erythropoietic protoporphyria

Estrogen insensitivity syndrome

Excess ovarian androgen release syndrome

Fabry Disease

Familial Amyloidosis, Finnish Type

Familial dysalbuminemic hyperthyroxinemia