Ovarian dysfunction (E28)

• ICD-10 Index

  • Endocrine, nutritional and metabolic diseases (E00–E90)

    • Disorders of other endocrine glands (E20-E35)

      • Ovarian dysfunction (E28)

        • E28 - Ovarian dysfunction NON-BILLABLE CODE
        • E28.0 - Estrogen excess BILLABLE CODE
        • E28.1 - Androgen excess BILLABLE CODE
        • E28.2 - Polycystic ovarian syndrome BILLABLE CODE
        • E28.3 - Primary ovarian failure NON-BILLABLE CODE
        • E28.31 - Premature menopause NON-BILLABLE CODE
        • E28.310 - Symptomatic premature menopause BILLABLE CODE
        • E28.319 - Asymptomatic premature menopause BILLABLE CODE
        • E28.39 - Other primary ovarian failure BILLABLE CODE
        • E28.8 - Other ovarian dysfunction BILLABLE CODE
        • E28.9 - Ovarian dysfunction, unspecified BILLABLE CODE

Clinical Information for Ovarian dysfunction (E28)

Eunuchism - The state of being a eunuch, a male without TESTES or whose testes failed to develop. It is characterized by the lack of mature male GERM CELLS and TESTICULAR HORMONES.

Hypogonadism - Condition resulting from deficient gonadal functions, such as GAMETOGENESIS and the production of GONADAL STEROID HORMONES. It is characterized by delay in GROWTH, germ cell maturation, and development of secondary sex characteristics. Hypogonadism can be due to a deficiency of GONADOTROPINS (hypogonadotropic hypogonadism) or due to primary gonadal failure (hypergonadotropic hypogonadism).

Kallmann Syndrome - A genetically heterogeneous disorder caused by hypothalamic GNRH deficiency and OLFACTORY NERVE defects. It is characterized by congenital HYPOGONADOTROPIC HYPOGONADISM and ANOSMIA, possibly with additional midline defects. It can be transmitted as an X-linked (GENETIC DISEASES, X-LINKED), an autosomal dominant, or an autosomal recessive trait.

Spinocerebellar Degenerations - A heterogenous group of degenerative syndromes marked by progressive cerebellar dysfunction either in isolation or combined with other neurologic manifestations. Sporadic and inherited subtypes occur. Inheritance patterns include autosomal dominant, autosomal recessive, and X-linked.

Prune Belly Syndrome - A syndrome characterized by abdominal wall musculature deficiency, cryptorchism, and urinary tract abnormalities. The syndrome derives its name from its characteristic distended abdomen with wrinkled skin.

Instructional Notations

Type 1 Excludes Type 1 Excludes
A type 1 excludes note is a pure excludes note. It means "NOT CODED HERE!" An Excludes1 note indicates that the code excluded should never be used at the same time as the code above the Excludes1 note. An Excludes1 is used when two conditions cannot occur together, such as a congenital form versus an acquired form of the same condition.

• isolated gonadotropin deficiency E23.0
• postprocedural ovarian failure E89.4