2007 ICD-9-CM Volume 1 Diagnosis Codes Home > Endocrine, Nutritional And Metabolic Diseases, And Immunity Disorders 240-279 > Diseases Of Other Endocrine Glands 250-259 >
 Other endocrine disorders- 259 is a non-specific code that cannot be used to specify a diagnosis
Delay in sexual development and puberty not elsewhere classified- Unusually late sexual maturity.
- 259.0 is a specific code that can be used to specify a diagnosis
- 259.0 contains 14 index entries
Precocious sexual development and puberty not elsewhere classified- Unusually early sexual maturity.
- 259.1 is a specific code that can be used to specify a diagnosis
- 259.1 contains 17 index entries
Carcinoid syndrome- A symptom complex associated with CARCINOID TUMOR and characterized by attacks of severe flushing of the skin, diarrheal watery stools, bronchoconstriction, sudden drops in blood pressure, edema, and ascites. The carcinoid tumors are usually located in the gastrointestinal tract and metastasize to the liver. Symptoms are caused by tumor secretion of serotonin, prostaglandins, and other biologically active substances. Cardiac manifestations constitute CARCINOID HEART DISEASE. (Dorland, 27th ed; Stedman, 25th ed)
- 259.2 is a specific code that can be used to specify a diagnosis
- 259.2 contains 23 index entries
Ectopic hormone secretion not elsewhere classified- 259.3 is a specific code that can be used to specify a diagnosis
- 259.3 contains 12 index entries
Dwarfism not elsewhere classified- The condition of being undersized as a result of premature arrest of skeletal growth. It may be caused by insufficient secretion of growth hormone (DWARFISM, PITUITARY).
- 259.4 is a specific code that can be used to specify a diagnosis
- 259.4 contains 6 index entries
Androgen insensitivity syndrome- 259.5 is a specific code that can be used to specify a diagnosis
- 259.5 contains 14 index entries
Other specified endocrine disorders- An abnormal congenital condition, associated with defects in the LAMIN TYPE A gene, which is characterized by premature aging in children, where all the changes of cell senescence occur. It is manifested by premature greying; hair loss; hearing loss (DEAFNESS); cataracts (CATARACT); ARTHRITIS; OSTEOPOROSIS; DIABETES MELLITUS; atrophy of subcutaneous fat; skeletal hypoplasia; elevated urinary HYALURONIC ACID; and accelerated ATHEROSCLEROSIS. Many affected individuals develop malignant tumors, especially SARCOMA.
- An autosomal recessive disorder that causes premature aging in adults, characterized by sclerodermal skin changes, cataracts, subcutaneous calcification, muscular atrophy, a tendency to diabetes mellitus, aged appearance of the face, baldness, and a high incidence of neoplastic disease.
- Werner Syndrome (WS) is an inherited disease characterized by an early onset of atherosclerosis, osteoporosis, diabetes mellitus, and cancers of non-epithelial cell origin. Cultured cells from WS patients also present a shortened replicative lifespan and increased genetic instability. The genomic instability of WS cells is manifested at the cytogenetic level in the form of chromosome breaks and translocations, and at the molecular level predominately by multiple, large DNA deletions. (J. Biol. Chem., 273(51):34139-34144, 1998)
- 259.8 is a specific code that can be used to specify a diagnosis
- 259.8 contains 42 index entries
Unspecified endocrine disorder- Pathological processes of the ENDOCRINE GLANDS, and diseases resulting from abnormal level of available HORMONES.
- 259.9 is a specific code that can be used to specify a diagnosis
- 259.9 contains 18 index entries
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