what is code for kallmann's syndrome in icd-9-cm

What is hypogonadotropic hypogonadism?

Definition. Hypogonadism is a condition in which the male testes or the female ovaries produce little or no sex hormones. Hypogonadotropic hypogonadism (HH) is a form of hypogonadism that is due to a problem with the pituitary gland or hypothalamus.

What does hypopituitarism mean?

Hypopituitarism is a rare disorder in which your pituitary gland fails to produce one or more hormones, or doesn't produce enough hormones. The pituitary gland is a kidney-bean-sized gland situated at the base of your brain.

What is the ICD-10 code for hypogonadotropic hypogonadism?

E23. 0 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2022 edition of ICD-10-CM E23. 0 became effective on October 1, 2021.

What is the ICD 9 code for estrogen deficiency?

256.39The correct ICD-9-CM code would be 256.39.

Is hypopituitarism the same as hypothyroidism?

Central hypothyroidism is much less common and is usually due to a tumor in the pituitary gland that disrupts its function and causes hypopituitarism. Hypopituitary patients may be deficient in one or more hormones, including thyroid hormone, growth hormone, cortisol, estrogen (women) or testosterone (men).

What is the most common cause of hypopituitarism?

Pituitary adenomas: One of the most common causes of primary hypopituitarism is a pituitary adenoma (a benign, or noncancerous, tumor).

What is diagnosis code E29?

Testicular dysfunctionICD-10 code E29 for Testicular dysfunction is a medical classification as listed by WHO under the range - Endocrine, nutritional and metabolic diseases .

Is hypogonadism the same as Testicular hypofunction?

Testicular hypofunction from the age of puberty onward may lead to testosterone deficiency, infertility, or both. Such hypofunction may be primary in the testes (primary hypogonadism) or secondary to deficiency of pituitary gonadotropic hormones (secondary hypogonadism).

What code is E23?

Hypofunction and other disorders of the pituitary gland.

What is code E28 39?

ICD-10 code E28. 39 for Other primary ovarian failure is a medical classification as listed by WHO under the range - Endocrine, nutritional and metabolic diseases .

What is menopausal and female climacteric states?

Globally, the term menopause is much more frequently used than climacteric but, before we use either one, we should consider that 'menopause' is referring to a specific event, the cessation of menses, and 'climacteric' to gradual changes of ovarian function that start before the menopause and continue thereafter for a ...

What does female climacteric state mean?

Climacteric is the period of life starting from the decline in ovarian activity until after the end of ovarian function. According to the definition, the period includes peri-menopause, menopause and post-menopause.

How to diagnose Kallmann syndrome?

Analysis of the olfactory bulbs by MRI can be useful, especially in young children. Genetic testing can also be used to diagnose the condition by identifying a disease-causing mutation in one of the genes responsible for Kallmann syndrome. [1]

What is Kallmann syndrome?

Listen. Kallmann syndrome (KS) is a condition that causes hypogonadotropic hypogonadism (HH) and an impaired sense of smell. HH affects the production of the hormones needed for sexual development. It is present from birth and is due to deficiency of gonadotropin-releasing hormone (GnRH). KS is often diagnosed at puberty due to lack ...

Why is KS diagnosed?

KS is often diagnosed at puberty due to lack of sexual development. It may first be suspected in infancy in males with undescended testicles or a small penis. Symptoms in untreated, adult males may include decreased bone density and muscle mass; small testicles; erectile dysfunction; low sex drive; and infertility.

Is Kallmann syndrome life threatening?

Kallmann syndrome (KS) is not a life-threatening condition. The main features are delayed or absent signs of puberty, and absent or diminished sense of smell (anosmia or hyposmia, respectively). Males with KS may have signs of the condition at birth, such as undescended testes or a smaller than average penis.

Can Kallmann syndrome cause fertility?

Fertility can be achieved in most cases. [1] [2] When the features of Kallmann syndrome are not accompanied by impaired sense of smell, the condition is referred to as idiopathic or isolated hypogonadotropic hypogonadism, or normosmic isolated GnRH deficiency (IGD). Last updated: 6/22/2016.

What is the defining feature of Kallmann syndrome?

Total lack of sense of smell ( anosmia) or markedly reduced sense of smell (hyposmia). This is the defining feature of Kallmann syndrome; it is not seen in other cases of HH. Approximately 50% of HH cases occur with anosmia and can be termed as Kallmann syndrome.

What is Kallmann syndrome?

Kallmann syndrome is a form of a group of conditions termed hypogonadotropic hypogonadism. To distinguish it from other forms of hypogonadotropic hypogonadism, Kallmann syndrome has the additional symptom of a total lack of sense of smell (anosmia) or a reduced sense of smell.

How many genes are involved in Kallmann syndrome?

The genetic and molecular basis of idiopathic hypogonadotropic hypogonadism. To date at least 25 different genes have been implicated in causing Kallmann syndrome or other forms of hypogonadotropic hypogonadism through a disruption in the production or activity of GnRH (37).

How old was Jimmy Scott when he got Kallman syndrome?

19 year old with Kallmann syndrome before diagnosis and treatment. Singer Jimmy Scott (r), whose unusual voice was due to Kallman syndrome. It is normally difficult to distinguish a case of Kallmann syndrome (KS)/hypogonadotropic hypogonadism (HH) from a straightforward constitutional delay of puberty.

Why do ovaries fail to function properly in KS/HH?

In most cases of KS/HH the testes and ovaries are able to function correctly, but fail to do so because they have not had the correct hormonal signals.

How long does it take for a baby to have a KS?

This is due to the human chorionic gonadotrophin (hCG) produced by placenta at approximately 12 to 20 weeks gestation (pregnancy) which is normally unaffected by having KS or CHH. People with KS/HH lack the surge of GnRH, LH, and FSH that normally occurs between birth and six months of age.

Who first described Kallmann syndrome?

Kallmann syndrome was first described by name in a paper published in 1944 by Franz Josef Kallmann, a German - American geneticist. The link between anosmia and hypogonadism had already been noted by Spanish doctor Aureliano Maestre de San Juan in 1856.