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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)

other metabolic and immunity disorders (270-279)

See also

v • d • eEndocrinepathology: endocrine diseases(E00-35, 240-259) ThyroidHypothyroidism(Iodine deficiency, Cretinism, Congenital hypothyroidism, Goitre, Myxedema) - Hyperthyroidism(Graves disease, Toxic multinodular goitre, Teratomawith thyroid tissue or Struma ovarii) - Thyroiditis(De Quervain's thyroiditis, Hashimoto's thyroiditis, Riedel's thyroiditis) - Euthyroid sick syndromePancreasDiabetes mellitus(type 1, type 2, coma, angiopathy, ketoacidosis, nephropathy, neuropathy, retinopathy, MODY) - Hypoglycemia- Hyperinsulinism- Zollinger-Ellison syndrome- insulin receptor (Rabson-Mendenhall 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- Pituitary apoplexyAdrenalCushing's syndrome(Nelson's syndrome, Pseudo-Cushing's syndrome) - CAH(Lipoid, 3β, 11β, 17α, 21α) - Hyperaldosteronism(Conn syndrome, Bartter syndrome) - Adrenal insufficiency(Addison's disease) - HypoaldosteronismGonadsovarian dysfunction (Polycystic ovary syndrome, Premature ovarian failure) - testicular dysfunction (5-alpha-reductase deficiency) - testosterone biosynthesis (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
v • d • eNutrition disorders(E40-68, 260-269) MalnutritionKwashiorkor- Marasmus- CatabolysisAvitaminosisB 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/OsteomalaciaMineraldeficiency Zinc deficiency- Iron deficiency- Magnesium deficiency- Chromium deficiencyHyperalimentationObesity- Vitamin poisoning(Hypervitaminosis A, Hypervitaminosis D, Hypervitaminosis E)
v • d • eInborn errorsof amino acid metabolism(E70-72, 270) KLysine/straight chain Glutaric acidemia type 1- type 2- Hyperlysinemia- Pipecolic acidemia- SaccharopinuriaLeucineMaple syrup urine disease- Isovaleric acidemia- 3-Methylcrotonyl-CoA carboxylase deficiency- 3-hydroxy-3-methylglutaryl-CoA lyase deficiency
G→pyruvate GlycineSarcosinemia- D-Glyceric acidemia- Glutathione synthetase deficiency
G→alpha-ketoglutarate Glutamate/glutamineSSADHDProlineHyperprolinemia- Prolidase deficiencyHistidineCarnosinemia- Histidinemia- Urocanic aciduria
G→succinyl-CoA MethionineHypermethioninemia- Homocystinuria- CystathioninuriaValineMaple syrup urine disease- Hypervalinemia- Isobutyryl-CoA dehydrogenase deficiencyIsoleucineMaple syrup urine disease- Beta-ketothiolase deficiency- 2-Methylbutyryl-CoA dehydrogenase deficiencyGeneral BC/OAPropionic acidemia- Methylmalonic acidemia
G→fumarate Phenylalanine/tyrosinePhenylketonuria: 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 • eInborn errorof carbohydrate metabolism(including glycogen storage diseases) (E73-74, 271) Disaccharidecatabolism Lactose intolerance- Sucrose intoleranceMonosaccharidecatabolism fructose: Essential fructosuria- Fructose intolerance
galactose/galactosemia : Galactokinase deficiency- Galactose-1-phosphate uridylyltransferase galactosemia- Galactose epimerase deficiencyMonosaccharidetransport Glucose-galactose malabsorption- Inborn errors of renal tubular transport(Renal glycosuria) GlycolysisGSD type VII, Tarui's, phosphofructokinase- Triosephosphate isomerase deficiency- Pyruvate kinase deficiencyPyruvatecatabolism PDHA- Fumarase deficiencyGluconeogenesisPCD- Fructose bisphosphatase deficiency- GSD type I, von Gierke, glucose 6-phosphataseGlycogenesisGSD type 0, glycogen synthase- GSD type IV, Andersen's, branchingGlycogenolysisGSD 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-phosphatasPentose phosphate pathwayGlucose-6-phosphate dehydrogenase deficiency- PentosuriaOther Hyperoxaluriasee also glycolysis enzymes, pentose phosphate pathway enzymes, fructose and galactose metabolism enzymes
v • d • eInborn errorof lipid metabolism- Lysosomal storage diseases- lipid storage disorders(E75, 272.7-272.8, 330.0-330.1) SphingolipidosesGangliosidoses: GM1 gangliosidoses, GM2 gangliosidoses(Sandhoff disease, Tay-Sachs disease, AB variant)

Fabry's disease - Gaucher's disease

sulfated: Leukodystrophy (Metachromatic leukodystrophy, Krabbe disease)

ceramide: Farber disease

phospholipid: Niemann-Pick diseaseNeuronal ceroid lipofuscinosisInfantile- Jansky-Bielschowsky disease- Batten diseaseOther Cerebrotendineous xanthomatosis- Cholesteryl ester storage disease(Wolman disease) see also glycolipid metabolism enzymes
v • d • eLipid metabolism disorders / Inborn errorof lipid metabolism- dyslipidemia(E78 and E71.3, 272) HyperlipidemiaHypercholesterolemia/Hypertriglyceridemia(Familial hypercholesterolemia, Combined hyperlipidemia) - XanthomaHypolipoproteinemiaHypoalphalipoproteinemia/HDL(Lecithin cholesterol acyltransferase deficiency, Tangier disease)
Hypobetalipoproteinemia/LDL(Abetalipoproteinemia, Apolipoprotein B deficiency) LipodystrophyBarraquer-Simons syndromeFatty acid metabolismdeficiency transport: Carnitine(Primary, I, II, -acylcarnitine) - Adrenoleukodystrophy

beta oxidation: Acyl CoA dehydrogenase (Short-chain, Medium-chain, Long-chain 3-hydroxy, Very long-chain) - Mitochondrial trifunctional protein deficiency

to acetyl-CoA: Malonic aciduriaCholesterolsynthesis Smith-Lemli-Opitz syndromeOther Sjögren-Larsson syndrome- Lipomatosis- Adiposis dolorosasee also lipid metabolism enzymes, lipoprotein metabolism
v • d • eInborn errors of metal metabolism(E83, 275) CuWilson's disease- Menkes diseaseFePrimary iron overload disorder: Haemochromatosis(Juvenile) - Aceruloplasminemia- AtransferrinemiaZnAcrodermatitis enteropathicaPO43−Hyperphosphatemia- Hypophosphatemia- HypophosphatasiaMg2+Hypermagnesemia- HypomagnesemiaCa2+Hypercalcaemia- Hypocalcaemia- Pseudohypoparathyroidism- PseudopseudohypoparathyroidismBiotin/MCDBiotinidase deficiency- Holocarboxylase synthetase deficiency
v • d • eWater-electrolyte imbalanceand acid-base imbalance(E86-E87, 276) Volume statusDehydration/Hypervolemia- HypovolemiaElectrolyteNa+ Hypernatremia/Hyponatremia

K+ Hyperkalemia/Hypokalemia

Cl− Hyperchloremia/HypochloremiaAcid-baseAcidosis: Metabolic- Respiratory- Lactic- Ketosis

Alkalosis: Metabolic, Respiratory

Mixed disorder of acid-base balance
v • d • eInborn errors of purine-pyrimidine metabolism(E79, 277.2) Purine metabolismAnabolism Adenylosuccinate lyase deficiencyNucleotide salvageLesch-Nyhan syndrome/Hyperuricemia- Adenine phosphoribosyltransferase deficiencyCatabolism Adenosine deaminase deficiency- Purine nucleoside phosphorylase deficiency- Xanthinuria- Gout
Pyrimidine metabolism Anabolism Orotic aciduriaCatabolism Dihydropyrimidine dehydrogenase deficiency
see also nucleotide metabolism, intermediates v • d • eHememetabolism disorders (E80, 277.1, 277.4) PorphyrinHepatic porphyria: Acute intermittent- Cutanea tarda/Hepatoerythropoietic- Hereditary copro-- Variegate
Erythropoietic: Gunther'sHereditary hyperbilirubinemiaUnconjugated: Lucey-Driscoll syndrome- Gilbert's syndrome- Crigler-Najjar syndrome
Conjugated: Dubin-Johnson syndrome- Rotor syndromesee also porphyrin metabolism enzymes, intermediates
v • d • eMetabolic disease: amyloidosis(E85, 277.3) Forms of amyloidSerum amyloid P component- Serum amyloid A- Transthyretin- Beta-2 microglobulin- Bence Jones protein/Multiple myeloma- Amyloid precursor protein/Amyloid betaSystemic amyloidosis AL amyloidosis- AA amyloidosis- Haemodialysis-associated amyloidosis- Senile systemic amyloidosis- Finnish type amyloidosis- Familial Mediterranean feverOrgan-limited amyloidosisheart (Cardiac amyloidosis) - brain (Familial amyloid neuropathy, Cerebral amyloid angiopathy, Alzheimer's disease)
v • d • eInborn errorof carbohydrate metabolism- Lysosomal storage diseases- glycosaminoglycanmetabolic pathology (E76, 277.5) Mucopolysaccharidosis
(Glycosaminoglycans) 1:Hurler/Scheie- 2:Hunter- 3:Sanfilippo ABCD- 4:Morquio- 6:Maroteaux-Lamy- 7:Sly
v • d • ePathology: Immune disorders(primarily D80-D89, 273, 279) Immunodeficiency/
primaryAntibody/humoral(B) Hypogammaglobulinemia/agammaglobulinemia(X-linked, Transient of infancy) - Dysgammaglobulinemia(IgA, IgG) - Common variable immunodeficiency- WHIM syndromeCell-mediated(T) DiGeorge syndrome- Nezelof syndrome- Purine nucleoside phosphorylase deficiencyCombined(B+T) Severe combined immunodeficiency(Adenosine deaminase deficiency, Omenn syndrome, X-SCID, ZAP70 deficiency) - Bare lymphocyte syndrome- Wiskott-Aldrich syndromeComplement deficiencyAngioedemaPBDchemotaxis/degranulation(Leukocyte adhesion deficiency, Chédiak-Higashi syndrome, Hyper-IgE syndrome)
respiratory burst(Chronic granulomatous disease, Myeloperoxidase deficiency) Other ICF syndrome
Immunoproliferative Hypergammaglobulinemia

Paraproteinemia (Cryoglobulinemia, Heavy chain disease, POEMS syndrome, Monoclonal gammopathy of undetermined significance)

Lymphoproliferative disorders (Sarcoidosis) Hypersensitivity Type I (Allergy) - Type II - Type III (Serum sickness) - Type IV (Contact dermatitis)
Autoimmunity/Autoimmune disease See also hematological malignancy and hematology v • d • eOther metabolicpathology/ Inborn error of metabolism(E70-90, 270-279) Other Alpha 1-antitrypsin deficiency- Cystic fibrosis- Acatalasia
Categories: Metabolic disorders | Immune system disorders | Medical manuals

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