icd 10 code for klinefelters syndrome

What is Klinefelter syndrome?

Klinefelter syndrome, unspecified. A form of male hypogonadism, characterized by the presence of an extra x chromosome, small testes, seminiferous tubule dysgenesis, elevated levels of gonadotropins, low serum testosterone, underdeveloped secondary sex characteristics, and male infertility (infertility, male).

What is the ICD 10 code for Turner syndrome?

Turner syndrome in fetus ICD-10-CM O35.1XX0 is grouped within Diagnostic Related Group (s) (MS-DRG v38.0): 817 Other antepartum diagnoses with o.r. Procedures with mcc 818 Other antepartum diagnoses with o.r. Procedures with cc

What is the ICD 10 code for chromosomal abnormality in fetus?

Maternal care for (suspected) chromosomal abnormality in fetus, not applicable or unspecified. O35.1XX0 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2019 edition of ICD-10-CM O35.1XX0 became effective on October 1, 2018.

What is the ICD 10 code for male diagnosis?

Q98.1 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 Q98.1 became effective on October 1, 2021. This is the American ICD-10-CM version of Q98.1 - other international versions of ICD-10 Q98.1 may differ. Q98.1 is applicable to male patients.

What is Klinefelter syndrome syndrome?

Klinefelter syndrome (sometimes called Klinefelter's, KS or XXY) is where boys and men are born with an extra X chromosome. Chromosomes are packages of genes found in every cell in the body. There are 2 types of chromosome, called the sex chromosomes, that determine the genetic sex of a baby.

What is another name for Klinefelter's syndrome?

Klinefelter syndrome is a genetic condition in which a boy is born with an extra X chromosome. Instead of the typical XY chromosomes in men, they have XXY, so this condition is sometimes called XXY syndrome.

What is Klinefelter syndrome XXY males?

Overview. Klinefelter syndrome is a genetic condition that results when a boy is born with an extra copy of the X chromosome. Klinefelter syndrome is a genetic condition affecting males, and it often isn't diagnosed until adulthood.

What are the different types of Klinefelter syndrome?

Several conditions resulting from the presence of more than one extra sex chromosome in each cell are sometimes described as variants of Klinefelter syndrome. These conditions include 48,XXXY syndrome, 48,XXYY syndrome, and 49,XXXXY syndrome.

Is Klinefelter syndrome trisomy or monosomy?

While a trisomy can occur with any chromosome, the condition is rarely viable. The major chromosomal aneuploidies are trisomy 13, trisomy 18, Turner Syndrome (45, X), Klinefelter syndrome (47, XXY), 47XYY, and 47XXX.

How do you diagnose Klinefelter syndrome?

Blood or urine samples can reveal abnormal hormone levels that are a sign of Klinefelter syndrome. Chromosome analysis. Also called karyotype analysis, this test is used to confirm a diagnosis of Klinefelter syndrome. A blood sample is sent to the lab to check the shape and number of chromosomes.

Can females have XXY syndrome?

Klinefelter syndrome affects males only; females cannot have it. Klinefelter syndrome results from a genetic abnormality in which males have an extra copy of the X chromosome. Instead of the usual XY chromosomes, males with Klinefelter syndrome have an XXY pattern.

Is Klinefelter syndrome an intersex condition?

2). Therefore, according to the NZKA, not all XXY individuals will develop Klinefelter Syndrome, for the Syndrome is simply a form of male hypogonadism, caused by a lack of testosterone: thus XXY is not an intersex condition.

How do you get Klinefelter syndrome?

Klinefelter syndrome is a condition that occurs in men as a result of an extra X chromosome. The most common symptom is infertility. Humans have 46 chromosomes, which contain all of a person's genes and DNA. Two of these chromosomes, the sex chromosomes, determine a person's gender.

Is Klinefelter syndrome a disability?

Most males with the 47,XXY karyotype have normal intelligence. Intellectual disability occurs in males with Klinefelter syndrome variants, who have a higher number of X chromosomes. About 70% of patients have minor developmental and learning disabilities.

The ICD code Q984 is used to code Klinefelter syndrome

Klinefelter syndrome or Klinefelter's syndrome (KS) (/ˈklaɪnfɛltər/) also known as 47,XXY or XXY, is the set of symptoms that result from two or more X chromosomes in males. The primary feature is sterility. Often symptoms may be subtle and many people do not realize they are affected.

MS-DRG Mapping

DRG Group #729-730 - Other male reproductive system diagnoses with CC or MCC.

ICD-10-CM Alphabetical Index References for 'Q98.4 - Klinefelter syndrome, unspecified'

The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code Q98.4. Click on any term below to browse the alphabetical index.

Equivalent ICD-9 Code GENERAL EQUIVALENCE MAPPINGS (GEM)

This is the official approximate match mapping between ICD9 and ICD10, as provided by the General Equivalency mapping crosswalk. This means that while there is no exact mapping between this ICD10 code Q98.4 and a single ICD9 code, 758.7 is an approximate match for comparison and conversion purposes.

The ICD code Q980 is used to code Klinefelter syndrome

Klinefelter syndrome or Klinefelter's syndrome (KS) (/ˈklaɪnfɛltər/) also known as 47,XXY or XXY, is the set of symptoms that result from two or more X chromosomes in males. The primary feature is sterility. Often symptoms may be subtle and many people do not realize they are affected.

MS-DRG Mapping

DRG Group #729-730 - Other male reproductive system diagnoses with CC or MCC.

ICD-10-CM Alphabetical Index References for 'Q98.0 - Klinefelter syndrome karyotype 47, XXY'

The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code Q98.0. Click on any term below to browse the alphabetical index.

Equivalent ICD-9 Code GENERAL EQUIVALENCE MAPPINGS (GEM)

This is the official approximate match mapping between ICD9 and ICD10, as provided by the General Equivalency mapping crosswalk. This means that while there is no exact mapping between this ICD10 code Q98.0 and a single ICD9 code, 758.7 is an approximate match for comparison and conversion purposes.