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  • List_of_ICD-9_codes_240-279:_Endocrine,_nutritional_and_metabolic_diseases,_and_immunity_disorders

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



Contents

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

disorders of thyroid gland (240-246)

diseases of other endocrine glands (250-259)

nutritional deficiencies (260-269)

  • (260) Kwashiorkor
  • (261) Nutritional marasmus
  • (262) Other severe protein-calorie malnutrition
  • (263) Other and unspecified protein-calorie malnutrition
  • (264) Vitamin A deficiency
    • (264.0) With conjunctival xerosis
    • (264.1) With conjunctival xerosis and Bitot's spot
    • (264.2) With corneal xerosis
    • (264.3) With corneal ulceration and xerosis
    • (264.4) With keratomalacia
    • (264.5) With night blindness
    • (264.6) With xerophthalmic scars of cornea
    • (264.7) Other ocular manifestations of vitamin A deficiency
    • (264.8) Other manifestations of vitamin A deficiency
    • (264.9) Unspecified vitamin A deficiency
  • (265) Thiamine and niacin deficiency states
  • (266) Deficiency of B-complex components
  • (267) Ascorbic acid deficiency
  • (268) Vitamin D deficiency
  • (269) Other nutritional deficiencies
    • (269.0) Deficiency of vitamin K
    • (269.1) Deficiency of other vitamins
    • (269.2) Unspecified vitamin deficiency
    • (269.3) Mineral deficiency, not elsewhere classified

other metabolic and immunity disorders (270-279)

See also

v • d • e
Endocrine pathology: endocrine diseases (E00-35, 240-259)
ThyroidHypothyroidism (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
PancreasDiabetes mellitus (type 1, type 2, coma, angiopathy, ketoacidosis, nephropathy, neuropathy, retinopathy) - Hypoglycemia - Hyperinsulinism - Zollinger-Ellison syndrome
ParathyroidHypoparathyroidism (Pseudohypoparathyroidism) - Hyperparathyroidism (Primary, Secondary, Tertiary)
PituitaryHyperpituitarism (Acromegaly, Hyperprolactinaemia, SIADH) - Hypopituitarism (Simmonds' disease/Sheehan's syndrome, Kallmann syndrome, Growth hormone deficiency, Diabetes insipidus) - Adiposogenital dystrophy - Empty sella syndrome
AdrenalCushing's syndrome (Nelson's syndrome, Pseudo-Cushing's syndrome) - CAH (due to 21-hydroxylase deficiency) - Hyperaldosteronism (Conn syndrome, Bartter syndrome) - Adrenal insufficiency (Addison's disease) - Hypoaldosteronism
Gonadsovarian dysfunction (Polycystic ovary syndrome, Premature ovarian failure) - testicular dysfunction (5-alpha-reductase deficiency) - general (Hypogonadism, Delayed puberty, Precocious puberty)
OtherAutoimmune polyendocrine syndrome - Carcinoid syndrome - Short stature (Laron syndrome, Psychogenic dwarfism) - Gigantism - Androgen insensitivity syndrome - Progeria - Multiple endocrine neoplasia (1, 2)
v • d • e
Nutritional pathology (E40-68, 260-269)
MalnutritionKwashiorkor - Marasmus
Other underconsumptionB 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: Zinc deficiency - Iron deficiency, Magnesium deficiency - Chromium deficiency
HyperalimentationObesity - Hypervitaminosis A - Hypervitaminosis D
v • d • e
Metabolic pathology / Inborn error of metabolism (E70-90, 270-279)
Amino acidAromatic (Phenylketonuria, Alkaptonuria, Ochronosis, Tyrosinemia, Albinism, Histidinemia) - Organic acidemias (Maple syrup urine disease, Propionic acidemia, Methylmalonic acidemia, Isovaleric acidemia, 3-Methylcrotonyl-CoA carboxylase deficiency) - Transport (Cystinuria, Cystinosis, Hartnup disease, Fanconi syndrome, Oculocerebrorenal syndrome) - Sulfur (Homocystinuria, Cystathioninuria) - Urea cycle disorder (N-Acetylglutamate synthase deficiency, Carbamoyl phosphate synthetase I deficiency, Ornithine transcarbamylase deficiency, Citrullinemia, Argininosuccinic aciduria, Hyperammonemia) - Glutaric acidemia type 1 - Hyperprolinemia - Sarcosinemia
CarbohydrateLactose intolerance - Glycogen storage disease (type I, type II, type III, type IV, type V, type VI, type VII) - fructose metabolism (Fructose intolerance, Fructose bisphosphatase deficiency, Essential fructosuria) - galactose metabolism (Galactosemia, Galactose-1-phosphate uridylyltransferase galactosemia, Galactokinase deficiency) - other intestinal carbohydrate absorption (Glucose-galactose malabsorption, Sucrose intolerance) - pyruvate metabolism and gluconeogenesis (PCD, PDHA) - Pentosuria - Renal glycosuria
Lipid storageSphingolipidoses/Gangliosidoses: GM2 gangliosidoses (Sandhoff disease, Tay-Sachs disease) - GM1 gangliosidoses - Mucolipidosis type IV - Gaucher's disease - Niemann-Pick disease - Farber disease - Fabry's disease - Metachromatic leukodystrophy - Krabbe disease
Neuronal ceroid lipofuscinosis (Batten disease) - Cerebrotendineous xanthomatosis - Cholesteryl ester storage disease (Wolman disease)
Fatty acid metabolismLipoprotein/lipidemias: Hyperlipidemia - Hypercholesterolemia - Familial hypercholesterolemia - Xanthoma - Combined hyperlipidemia - Lecithin cholesterol acyltransferase deficiency - Tangier disease - Abetalipoproteinemia
Fatty acid: Adrenoleukodystrophy - Acyl-coA dehydrogenase (Short-chain, Medium-chain, Long-chain 3-hydroxy, Very long-chain) - Carnitine (Primary, I, II)
MineralCu Wilson's disease/Menkes disease - Fe Haemochromatosis - Zn Acrodermatitis enteropathica - PO43�' Hypophosphatemia/Hypophosphatasia - Mg2+ Hypermagnesemia/Hypomagnesemia - Ca2+ Hypercalcaemia/Hypocalcaemia/Disorders of calcium metabolism
Fluid, electrolyte
and acid-base balance		Electrolyte disturbance - Na+ Hypernatremia/Hyponatremia - Acidosis (Metabolic, Respiratory, Lactic) - Alkalosis (Metabolic, Respiratory) - Mixed disorder of acid-base balance - H2O Dehydration/Hypervolemia - K+ Hypokalemia/Hyperkalemia - Cl�' Hyperchloremia/Hypochloremia
Purine and pyrimidineHyperuricemia - Lesch-Nyhan syndrome - Xanthinuria
PorphyrinAcute intermittent, Gunther's, Cutanea tarda, Erythropoietic, Hepatoerythropoietic, Hereditary copro-, Variegate
BilirubinUnconjugated (Lucey-Driscoll syndrome, Gilbert's syndrome, Crigler-Najjar syndrome) - Conjugated (Dubin-Johnson syndrome, Rotor syndrome)
GlycosaminoglycanMucopolysaccharidosis - 1:Hurler/Hunter - 3:Sanfilippo - 4:Morquio - 6:Maroteaux-Lamy - 7:Sly
GlycoproteinMucolipidosis - I-cell disease - Pseudo-Hurler polydystrophy - Aspartylglucosaminuria - Fucosidosis - Alpha-mannosidosis - Sialidosis
OtherAlpha 1-antitrypsin deficiency - Cystic fibrosis - Amyloidosis (Familial Mediterranean fever) - Acatalasia
v • d • e
Pathology: Immune disorders (primarily D80-D89, 273, 279)
Antibody defectsX-linked agammaglobulinemia - Selective immunoglobulin A deficiency
Combined immunodeficienciesSevere combined immunodeficiency (X-SCID) - Adenosine deaminase deficiency - Nezelof syndrome - Purine nucleoside phosphorylase deficiency - Bare lymphocyte syndrome
OtherWiskott-Aldrich syndrome - DiGeorge syndrome - Hyper-IgE syndrome - Common variable immunodeficiency - Complement deficiency (Angioedema) - Sarcoidosis - Hypergammaglobulinemia - Cryoglobulinemia - Paraproteinemia - Immunodeficiency/Primary immunodeficiency
Autoimmunitysee list of autoimmune diseases
 
This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "List_of_ICD-9_codes_240-279:_Endocrine,_nutritional_and_metabolic_diseases,_and_immunity_disorders". A list of authors is available in Wikipedia.
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