List of ICD-9 codes 240-279: Endocrine, nutritional and metabolic diseases, and immunity disorders

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1 3. Endocrine, nutritional and metabolic diseases, and immunity disorders (240-279)
2 See also

3. Endocrine, nutritional and metabolic diseases, and immunity disorders (240-279)

Pituitary	Hyperpituitarism (Acromegaly, Hyperprolactinaemia, SIADH) Hypopituitarism (Sheehan's syndrome, Kallmann syndrome, Growth hormone deficiency, Diabetes insipidus) Adiposogenital dystrophy - Empty sella syndrome - Pituitary apoplexy - ACTH deficiency

Thyroid	Hypothyroidism (Iodine deficiency, Cretinism, Congenital hypothyroidism, Goitre, Myxedema) Hyperthyroidism (Graves disease, Toxic multinodular goitre, Teratoma with thyroid tissue or Struma ovarii) Thyroiditis (De Quervain's thyroiditis, Hashimoto's thyroiditis, Riedel's thyroiditis) Euthyroid sick syndrome - Thyroid hormone resistance - Thyroid nodule

Parathyroid	Hypoparathyroidism (Pseudohypoparathyroidism) - Hyperparathyroidism (Primary, Secondary, Tertiary)

Adrenal	Adrenocortical hyperfunction: Cushing's syndrome (Nelson's syndrome, Pseudo-Cushing's syndrome) - Hyperaldosteronism (Conn syndrome, Bartter syndrome) CAH (Lipoid, 3β, 11β, 17α, 21α) Adrenal insufficiency (Addison's disease, Waterhouse-Friderichsen syndrome) - Hypoaldosteronism

Gonads	ovarian (Polycystic ovary syndrome, Premature ovarian failure) testicular (5-alpha-reductase deficiency, 17-beta-hydroxysteroid dehydrogenase deficiency) general (Hypogonadism, Delayed puberty, Precocious puberty)

Other

Androgen insensitivity syndrome - Autoimmune polyendocrine syndrome - Carcinoid syndrome - Gigantism - Short stature (Laron syndrome, Psychogenic dwarfism) - Multiple endocrine neoplasia (1, 2) - Progeria - Woodhouse-Sakati syndrome - thymus (Abscess of thymus, Thymus hyperplasia)

see also congenital, neoplasia

v • d • e Nutrition disorders (E40-68, 260-269)

Malnutrition	Kwashiorkor - Marasmus - Catabolysis

Avitaminosis	B vitamins: B1: Beriberi/Wernicke's encephalopathy, B2: Ariboflavinosis, B3: Pellagra, B6: Pyridoxine deficiency, B7: Biotin deficiency, B9: Folate deficiency, B12: Vitamin B12 deficiency other vitamins: A: Vitamin A deficiency/Bitot's spots, C: Scurvy, D: Rickets/Osteomalacia

Mineral deficiency	Zinc deficiency - Iron deficiency - Magnesium deficiency - Chromium deficiency - Keshan disease

Hyperalimentation	Obesity - Vitamin poisoning (Hypervitaminosis A, Hypervitaminosis D, Hypervitaminosis E)

v • d • e

Inborn errors of amino acid metabolism (E70-72, 270)

Lysine/straight chain	Glutaric acidemia type 1 - type 2 - Hyperlysinemia - Pipecolic acidemia - Saccharopinuria

Leucine	Maple syrup urine disease - Isovaleric acidemia - 3-Methylcrotonyl-CoA carboxylase deficiency - 3-hydroxy-3-methylglutaryl-CoA lyase deficiency

G→pyruvate

Glycine

Sarcosinemia - D-Glyceric acidemia - Glutathione synthetase deficiency

G→alpha-ketoglutarate

Glutamate/glutamine	SSADHD

Proline	Hyperprolinemia - Prolidase deficiency

Histidine	Carnosinemia - Histidinemia - Urocanic aciduria

G→succinyl-CoA


Methionine	Hypermethioninemia - Homocystinuria - Cystathioninuria

Valine	Maple syrup urine disease - Hypervalinemia - Isobutyryl-CoA dehydrogenase deficiency

Isoleucine	Maple syrup urine disease - Beta-ketothiolase deficiency - 2-Methylbutyryl-CoA dehydrogenase deficiency

General BC/OA	Propionic acidemia - Methylmalonic acidemia

G→fumarate


Phenylalanine/tyrosine	Phenylketonuria: Tetrahydrobiopterin deficiency - 6-Pyruvoyltetrahydropterin synthase deficiency Tyrosinemia: Type II tyrosinemia - Type III tyrosinemia/Hawkinsinuria - Alkaptonuria/Ochronosis - Type I tyrosinemia

G→oxaloacetate


Urea cycle/Hyperammonemia (arginine, aspartate)	N-Acetylglutamate synthase deficiency - Carbamoyl phosphate synthetase I deficiency - Ornithine transcarbamylase deficiency/translocase deficiency - Citrullinemia - Argininosuccinic aciduria - Argininemia

Transport

Cystinuria - Hartnup disease - Oculocerebrorenal syndrome - Lysinuric protein intolerance - Inborn errors of renal tubular transport (Cystinosis, Fanconi syndrome)

Tyrosine→Melanin

Albinism: Ocular albinism - Oculocutaneous albinism (Hermansky-Pudlak syndrome) - Waardenburg syndrome

Glycine→Creatine

GAMT deficiency

Other

Trimethylaminuria - 2-Hydroxyglutaric aciduria - Fumarase deficiency

see also Amino acid metabolism enzymes, Urea cycle enzymes, intermediates

v • d • e Inborn error of carbohydrate metabolism (including glycogen storage diseases) (E73-74, 271)

Disaccharide catabolism	Lactose intolerance - Sucrose intolerance

Monosaccharide catabolism	fructose: Essential fructosuria - Fructose intolerance galactose/galactosemia : Galactokinase deficiency - Galactose-1-phosphate uridylyltransferase galactosemia - Galactose epimerase deficiency

Monosaccharide transport	Glucose-galactose malabsorption - Inborn errors of renal tubular transport (Renal glycosuria)

Glycolysis	GSD type VII, Tarui's, phosphofructokinase - Triosephosphate isomerase deficiency - Pyruvate kinase deficiency

Pyruvate catabolism	PDHA - Fumarase deficiency

Gluconeogenesis	PCD - Fructose bisphosphatase deficiency - GSD type I, von Gierke, glucose 6-phosphatase

Glycogenesis	GSD type 0, glycogen synthase - GSD type IV, Andersen's, branching

Glycogenolysis	GSD type II, Pompe's, glucosidase - GSD type III, Cori's, debranching - GSD type V, McArdle, glycogen phosphorylase/GSD type VI, Hers', glycogen phosphorylase - GSD type I, von Gierke, glucose 6-phosphatase

Pentose phosphate pathway	Glucose-6-phosphate dehydrogenase deficiency - Pentosuria

Other	Hyperoxaluria (Primary hyperoxaluria)

see also glycolysis enzymes, pentose phosphate pathway enzymes, fructose and galactose metabolism enzymes

v • d • e

Inborn error of lipid metabolism - Lysosomal storage diseases - lipid storage disorders (E75, 272.7-272.8, 330.0-330.1)

Sphingolipidoses

Gangliosidoses	GM1 gangliosidoses GM2 gangliosidoses (Sandhoff disease, Tay-Sachs disease, AB variant)

Sulfatidoses	Multiple sulfatase deficiency - Metachromatic leukodystrophy

Other	Fabry's disease - Gaucher's disease sulfated: Leukodystrophy (Krabbe disease) ceramide: Farber disease phospholipid: Niemann-Pick disease

Neuronal ceroid lipofuscinosis

Infantile - Jansky-Bielschowsky disease - Batten disease

Other

Cerebrotendineous xanthomatosis - Cholesteryl ester storage disease (Wolman disease)

see also glycolipid metabolism enzymes

v • d • e Lipid metabolism disorders / Inborn error of lipid metabolism - dyslipidemia (E78 and E71.3, 272)

Hyperlipidemia	Hypercholesterolemia/Hypertriglyceridemia (Familial hypercholesterolemia, Combined hyperlipidemia) - Xanthoma

Hypolipoproteinemia	Hypoalphalipoproteinemia/HDL (Lecithin cholesterol acyltransferase deficiency, Tangier disease) Hypobetalipoproteinemia/LDL (Abetalipoproteinemia, Apolipoprotein B deficiency)

Lipodystrophy

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