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

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[edit] 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

Pathology: Medical conditions and ICD code
(Disease / Disorder / Illness, 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
Acid-base
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
General
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)
Genetic disorder, organelle: Peroxisomal disorders and lysosomal structural disorders (E80.3, 277.86)
Peroxisome biogenesis disorder
Enzyme-related
Transporter-related
Lysosomal
B structural (perx, skel, cili, mito, nucl, sclr) · DNA/RNA/protein synthesis (drep, trfc, tscr, tltn) · membrane (icha, slcr, atpa, abct, othr) · transduction (iter, csrc, itra), trfk
Carbohydrate metabolism
PCD · PDHA
Primarily nervous system
LHON · NARP · Leigh's
Myopathies
No primary system
Chromosomal
B structural (perx, skel, cili, mito, nucl, sclr) · DNA/RNA/protein synthesis (drep, trfc, tscr, tltn) · membrane (icha, slcr, atpa, abct, othr) · transduction (iter, csrc, itra), trfk
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
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