icd 10 code for kallmann syndrome

What is the abbreviation for Kallmann syndrome?

Kallmann syndrome. Kallmann syndrome ( KS) is a genetic disorder that prevents a person from starting or fully completing puberty. 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...

What is the PMC code for Kallmann syndrome?

PMC 3473216. PMID 23015291. National Organisation for Rare Diseases page on Kallmann syndrome.

How many genes are involved in Kallmann syndrome?

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).

What is the ICD 10 code for Angelman syndrome?

Angelman syndrome 1 Q93.51 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. 2 The 2021 edition of ICD-10-CM Q93.51 became effective on October 1, 2020. 3 This is the American ICD-10-CM version of Q93.51 - other international versions of ICD-10 Q93.51 may differ. More ...

What code is E23?

Hypofunction and other disorders of the pituitary gland.

What is the difference between Hypopituitarism and Panhypopituitarism?

The pituitary makes hormones that are needed for normal body functions. When you do not have two or more of the pituitary hormones, it is known as hypopituitarism (hahy-poh-pi-too-i-tuh-riz-uh m). The lack of all pituitary hormones is known as panhypopituitarism.

What is ICD-10 testicular hypofunction?

ICD-10 code E29. 1 for Testicular hypofunction is a medical classification as listed by WHO under the range - Endocrine, nutritional and metabolic diseases .

What is the ICD 10 code for hormone disorder?

ICD-10-CM Code for Endocrine disorder, unspecified E34. 9.

What is the ICD 10 code for panhypopituitarism?

E23. 0 - Hypopituitarism. ICD-10-CM.

What is Simmonds syndrome?

Simmonds' disease or pituitary cachexia is a syndrome ascribed to destruction or physiological exhaustion of the hypophysis (chiefly the anterior portion). The destruction may be caused by embolic infarction, tumor, syphilis, tuberculosis, metastatic abscesses, inflammation, etc.

Is Testicular Hypofunction the same as hypogonadism?

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 is the ICD-10 code for male hypogonadism?

E29. 1 - Testicular hypofunction. ICD-10-CM.

What is the CPT code for testicular hypofunction?

Group 1CodeDescriptionE29.1Testicular hypofunctionE29.8Other testicular dysfunctionE89.5Postprocedural testicular hypofunctionN50.89Other specified disorders of the male genital organs7 more rows

What is the ICD10 code for Kallmann Syndrome? And the ICD9 code for Kallmann Syndrome?

E23.0 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. This is the American ICD-10-CM version of E23.0. Other international versions of ICD-10 E23.0 may differ. Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.

Stories of Kallmann Syndrome

What can you say my story of how I was born as an http://en.wikipedia.org/wiki/Intersex/DSD person and living my life is as unique as the next person. I’m no different from anyone else, other than being born with an Intersex/ DSD (http://en.wikipe...

Kallmann Syndrome forum

We are currently seeking research participants who have been diagnosed with idiopathic hypogonadotropic hypogonadism (IHH), including Kallmann Syndrome (KS), for such a study. This study is being run through the Pennsylvania State University De...

Attention

Only comments seeking to improve the quality and accuracy of information on the Orphanet website are accepted. For all other comments, please send your remarks via contact us. Only comments written in English can be processed.

Epidemiology

The prevalence is estimated at 1/8,000 males and 1/40,000 females, but is probably underestimated.

Clinical description

Most cases are diagnosed at the time of puberty due to lack of sexual development, but KS may also be suspected in infancy in males with cryptorchidism, micropenis or associated non reproductive signs.

Etiology

KS is caused by impaired development of the olfactory system and disrupted embryonic migration of the GnRH-synthesizing neurons from the olfactory epithelium to the hypothalamic region of the brain. The majority of reported cases are sporadic but familial forms have been described.

Diagnostic methods

Diagnostic methods consist of hormone evaluation (sex steroids, gonadal peptides and pituitary gonadotropin dosage), as well as evaluation of the sense of smell (olfactometry). Morphological analysis of the olfactory bulbs by MRI can be useful, especially in young children.

Differential diagnosis

Differential diagnoses include isolated congenital gonadotropin deficiency and CHARGE syndrome (see these terms).

Antenatal diagnosis

In a familial context of FGFR1, FGF8, KAL1, or CHD7 mutations, bone abnormalities, cleft lip/palate, renal agenesis, or multiple developmental defects can be found in the fetus by ultrasonography.

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.

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.

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 males with KS/CHH have infertility?

In males with KS/CHH, infertility is primarily due to the lack of sperm production within the testes. Sperm production can be achieved through either the use of GnRH administered via a microinfusion pump or through the use of gonadotropin injections ( hCG, FSH, hMG ).

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.