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

From Wikipedia, the free encyclopedia
Jump to: navigation, search

Contents

3. Endocrine, nutritional and metabolic diseases, and immunity disorders (240–279) [edit]

Disorders of thyroid gland (240–246) [edit]

Diseases of other endocrine glands (249–259) [edit]

Nutritional deficiencies (260–269) [edit]

Other metabolic and immunity disorders (270–279) [edit]

Disorders of amino-acid transport and metabolism [edit]

Disorders of carbohydrate transport and metabolism [edit]

Disorders of lipoid metabolism [edit]

Disorders of plasma protein metabolism [edit]

Gout [edit]

Disorders of mineral metabolism [edit]

Disorders of fluid, electrolyte, and acid-base balance [edit]

Other and unspecified disorders of metabolism [edit]

Obesity and other hyperalimentation [edit]

Disorders involving the immune mechanism [edit]

See also [edit]

Pathology: Medical conditions and ICD code
(Disease / Disorder / Syndrome / Sequence, Symptom / Sign, Injury, etc.)
(A/B, 001–139)
(C/D,
140–239 &
279–289)
(E, 240–278)
(F, 290–319)
(G, 320–359)
(H, 360–389)
(I, 390–459)
(J, 460–519)
(K, 520–579)
(L, 680–709)
(M, 710–739)
(N, 580–629)
(O, 630–679)
(P, 760–779)
(Q, 740–759)
(R, 780–799)
(S/T, 800–999)
Hypoalimentation/
malnutrition
Other
vitamins
Hyperalimentation
Mineral overload

M: NUT

cof, enz, met

drug (A8/11/12)
K→acetyl-CoA
Lysine/straight chain
G
General BC/OA
Transport/
IE of RTT
Other

M: MET

mt, k, c/g/r/p/y/i, f/h/s/l/o/e, a/u, n, m

k, cgrp/y/i, f/h/s/l/o/e, au, n, m, epon

m (A16/C10), i (k, c/g/r/p/y/i, f/h/s/o/e, a/u, n, m)
Sucrose, transport
(extracellular)
Disaccharide catabolism
Monosaccharide transport
Hexose → glucose
Monosaccharide catabolism
Glucose ⇄ glycogen
Glucose ⇄ CAC
Pentose phosphate pathway
Other

M: MET

mt, k, c/g/r/p/y/i, f/h/s/l/o/e, a/u, n, m

k, cgrp/y/i, f/h/s/l/o/e, au, n, m, epon

m (A16/C10), i (k, c/g/r/p/y/i, f/h/s/o/e, a/u, n, m)
Hyperlipidemia
Hypolipoproteinemia
Lipodystrophy
Other

M: MET

mt, k, c/g/r/p/y/i, f/h/s/l/o/e, a/u, n, m

k, cgrp/y/i, f/h/s/l/o/e, au, n, m, epon

m (A16/C10), i (k, c/g/r/p/y/i, f/h/s/o/e, a/u, n, m)
Anabolism
Post-translational modification
of lysosomal enzymes
Catabolism
Other

M: MET

mt, k, c/g/r/p/y/i, f/h/s/l/o/e, a/u, n, m

k, cgrp/y/i, f/h/s/l/o/e, au, n, m, epon

m (A16/C10), i (k, c/g/r/p/y/i, f/h/s/o/e, a/u, n, m)
Sphingolipidoses
(to ceramide)
NCL
Other

M: MET

mt, k, c/g/r/p/y/i, f/h/s/l/o/e, a/u, n, m

k, cgrp/y/i, f/h/s/l/o/e, au, n, m, epon

m (A16/C10), i (k, c/g/r/p/y/i, f/h/s/o/e, a/u, n, m)
PCDs/PP
Other hypergammaglobulinemia
Transition metal
Electrolyte
Na+ and K+
deficiency: Hypomagnesemia

M: NUT

cof, enz, met

drug (A8/11/12)
Volume status
Electrolyte
Na+
K+
Cl−
Acid-base
Acidosis
Alkalosis
Both
Purine metabolism
Anabolism
Catabolism
Pyrimidine metabolism
Anabolism
Catabolism

M: MET

mt, k, c/g/r/p/y/i, f/h/s/l/o/e, a/u, n, m

k, cgrp/y/i, f/h/s/l/o/e, au, n, m, epon

m (A16/C10), i (k, c/g/r/p/y/i, f/h/s/o/e, a/u, n, m)
Heme metabolism disorders (E80, 277.1, 277.4)
Porphyria,
hepatic and erythropoietic
(porphyrin)
Hereditary hyperbilirubinemia
(bilirubin)

M: MET

mt, k, c/g/r/p/y/i, f/h/s/l/o/e, a/u, n, m

k, cgrp/y/i, f/h/s/l/o/e, au, n, m, epon

m (A16/C10), i (k, c/g/r/p/y/i, f/h/s/o/e, a/u, n, m)
Common amyloid forming proteins
Systemic amyloidosis
Organ-limited amyloidosis
Anabolism
Catabolism

M: MET

mt, k, c/g/r/p/y/i, f/h/s/l/o/e, a/u, n, m

k, cgrp/y/i, f/h/s/l/o/e, au, n, m, epon

m (A16/C10), i (k, c/g/r/p/y/i, f/h/s/o/e, a/u, n, m)
Synthesis
Degradation
Acyl transport
Beta oxidation
General
Unsaturated
Odd chain
Other
To acetyl-CoA
Aldehyde

M: MET

mt, k, c/g/r/p/y/i, f/h/s/l/o/e, a/u, n, m

k, cgrp/y/i, f/h/s/l/o/e, au, n, m, epon

m (A16/C10), i (k, c/g/r/p/y/i, f/h/s/o/e, a/u, n, m)
Genetic disorder, organelle: Peroxisomal disorders and lysosomal structural disorders (E80.3, 277.86)
Peroxisome biogenesis disorder
Enzyme-related
Transporter-related
Lysosomal
Carbohydrate metabolism
PCD · PDHA
Primarily nervous system
LHON · NARP · Leigh's
Myopathies
No primary system
Chromosomal
WHO-I/Langerhans cell histiocytosis/
X-type histiocytosis
WHO-II/non-Langerhans cell histiocytosis/
Non-X histiocytosis
WHO-III/malignant histiocytosis
Ungrouped
Primary
Other
Acquired
Leukopenia:
Lymphocytopenia
Complement deficiency
Other
Retrieved from "http://en.wikipedia.org/w/index.php?title=List_of_ICD-9_codes_240–279:_endocrine,_nutritional_and_metabolic_diseases,_and_immunity_disorders&oldid=551304393"