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

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

disorders of thyroid gland (240-246)

diseases of other endocrine glands (249-259)

nutritional deficiencies (260-269)

other metabolic and immunity disorders (270-279)

Disorders of amino-acid transport and metabolism

Disorders of carbohydrate transport and metabolism

Disorders of lipoid metabolism

Disorders of plasma protein metabolism

Gout

Disorders of mineral metabolism

Disorders of fluid, electrolyte, and acid-base balance

Other and unspecified disorders of metabolism

Obesity and other hyperalimentation

Disorders involving the immune mechanism

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 & 280-289)
(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
Hyperalimentation
Mineral overload

M: NUT

cof, enz

drug(A8/11/12)

K→acetyl-CoA
Lysine/straight chain
G
General BC/OA
Transport/
IE of RTT
Other

M: MET

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

au/y/n/h, rgcp/i, f/s/l/o, m, epon

meds(A16, C10),intm(a/u/y/n/h, r/g/c/p/i, f/s/o)

Sucrose, transport
(extracellular)
Disaccharide catabolism
Monosaccharide transport
Hexose → glucose
Monosaccharide catabolism
Glucose ⇄ glycogen
Glucose ⇄ CAC
Pyruvate catabolism
Pentose phosphate pathway
Other

M: MET

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

au/y/n/h, rgcp/i, f/s/l/o, m, epon

meds(A16, C10),intm(a/u/y/n/h, r/g/c/p/i, f/s/o)

Hyperlipidemia
Hypolipoproteinemia
Lipodystrophy
Other

M: MET

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

au/y/n/h, rgcp/i, f/s/l/o, m, epon

meds(A16, C10),intm(a/u/y/n/h, r/g/c/p/i, f/s/o)

Post-translational modification
of lysosomal enzymes
Glycoprotein degradation
Other

M: MET

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

au/y/n/h, rgcp/i, f/s/l/o, m, epon

meds(A16, C10),intm(a/u/y/n/h, r/g/c/p/i, f/s/o)

Sphingolipidoses
(to ceramide)
NCL
Other

M: MET

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

au/y/n/h, rgcp/i, f/s/l/o, m, epon

meds(A16, C10),intm(a/u/y/n/h, r/g/c/p/i, f/s/o)

PCDs/PP
Other hypergammaglobulinemia
Transition metal
Electrolyte

M: MET

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

au/y/n/h, rgcp/i, f/s/l/o, m, epon

meds(A16, C10),intm(a/u/y/n/h, r/g/c/p/i, f/s/o)

Volume status
Electrolyte
Acid-base
Both
Purine metabolism
Anabolism
Catabolism
Pyrimidine metabolism
Anabolism
Catabolism

M: MET

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

au/y/n/h, rgcp/i, f/s/l/o, m, epon

meds(A16, C10),intm(a/u/y/n/h, r/g/c/p/i, f/s/o)

Heme metabolism disorders (E80, 277.1, 277.4)
Porphyria,
hepatic and erythropoietic
(porphyrin)
Hereditary hyperbilirubinemia
(bilirubin)

M: MET

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

au/y/n/h, rgcp/i, f/s/l/o, m, epon

meds(A16, C10),intm(a/u/y/n/h, r/g/c/p/i, f/s/o)

Common amyloid forming proteins
Systemic amyloidosis
Organ-limited amyloidosis
Anabolism
Catabolism

M: MET

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

au/y/n/h, rgcp/i, f/s/l/o, m, epon

meds(A16, C10),intm(a/u/y/n/h, r/g/c/p/i, f/s/o)

Synthesis
Degradation
General
Other

M: MET

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

au/y/n/h, rgcp/i, f/s/l/o, m, epon

meds(A16, C10),intm(a/u/y/n/h, r/g/c/p/i, f/s/o)

Zellweger spectrum
Other
Carbohydrate metabolism
PCD · PDHA
Primarily nervous system
LHON · NARP · Leigh's
Myopathies
No primary system
WHO-I/Langerhans cell histiocytosis
WHO-II/non-Langerhans cell histiocytosis
WHO-III/malignant histiocytosis
Ungrouped
Primary
Other
Acquired
Leukopenia:
Lymphocytopenia
Complement deficiency
Other
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