2009 ICD-9-CM Diagnosis 259.* : Other endocrine disorders

Free ICD-9-CM Diagnosis Codes Lookup > 2009 > Endocrine, Nutritional And Metabolic Diseases, And Immunity Disorders 240-279 > Diseases Of Other Endocrine Glands 249-259 > Other endocrine disorders 259.* > 
2009 ICD-9-CM Diagnosis Code 259 Other endocrine disorders
2009 ICD-9-CM Diagnosis Code 259.0Delay in sexual development and puberty not elsewhere classified
Unusually late sexual maturity.
2009 ICD-9-CM Diagnosis Code 259.1Precocious sexual development and puberty not elsewhere classified
unusually early sexual maturity.
2009 ICD-9-CM Diagnosis Code 259.2Carcinoid syndrome
2009 ICD-9-CM Diagnosis Code 259.3Ectopic hormone secretion not elsewhere classified
2009 ICD-9-CM Diagnosis Code 259.4Dwarfism not elsewhere classified
condition of being undersized as a result of premature arrest of skeletal growth.
2009 ICD-9-CM Diagnosis Code 259.5 Androgen insensitivity syndrome
2009 ICD-9-CM Diagnosis Code 259.50Androgen insensitivity, unspecified 
2009 ICD-9-CM Diagnosis Code 259.51Androgen insensitivity syndrome
aspects of female morphology in a XY genotype caused by defects in cellular receptors for testosterone and dihydrotestosterone, transmitted as an x-linked trait.
Sexual ambiguity in males due to a sexual differentiation disorder caused by testicular failure to respond to androgens. The affected males have abdominal and inguinal testes, female external genitalia and breasts, blind vaginas, and absent uteri. Some patients have absent pubic and axillary hair, hence the synonym "hairless pseudofemale." Mental retardation occurs in some cases.
2009 ICD-9-CM Diagnosis Code 259.52Partial androgen insensitivity
2009 ICD-9-CM Diagnosis Code 259.8Other specified endocrine disorders
autosomal recessive disorder that causes premature aging in adults, characterized by sclerodermal skin changes, cataracts, subcutaneous calcifications, 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)
2009 ICD-9-CM Diagnosis Code 259.9Unspecified endocrine disorder
impairment of health or a condition of abnormal functioning of the system of glands that release their secretions (hormones) directly into the circulatory system.
Any deviation from the normal structure or function of the endocrine system that is manifested by a characteristic set of symptoms and signs. (NCI)
Any deviation from the normal structure or function of the endocrine system that is manifested by a characteristic set of symptoms and signs.
 258.*