icd 10 code for trisomy 18

by Johnpaul Bailey 3 min read

ICD-10 code Q91. 3 for Trisomy 18, unspecified is a medical classification as listed by WHO under the range - Congenital malformations, deformations and chromosomal abnormalities .

What is Z13 89?

Code Z13. 89, encounter for screening for other disorder, is the ICD-10 code for depression screening.

What is the ICD-10 CM code for maternal care for suspected chromosomal abnormality in the fetus?

ICD-10-CM Code for Maternal care for (suspected) chromosomal abnormality in fetus O35. 1.

Is Edwards Syndrome genetic?

Edwards syndrome (trisomy 18) is a genetic condition that causes physical growth delays during fetal development. Life expectancy for children diagnosed with Edwards syndrome is short due to several life-threatening complications of the condition.

What is the ICD-10 code for trisomy 21?

ICD-10 code Q90. 2 for Trisomy 21, translocation is a medical classification as listed by WHO under the range - Congenital malformations, deformations and chromosomal abnormalities .

What is the ICD-10 code for advanced maternal age?

O09. 521 is applicable to maternity patients aged 12 - 55 years inclusive.

Do babies with trisomy 18 suffer?

Most babies with trisomy 18 have problems that affect all parts of the body. Heart problems, feeding problems, and infections are what most often lead to death.

Does trisomy 18 affect more males or females?

Trisomy 18 affects females more frequently than males by a ratio of three or four to one. Large population surveys indicate that it occurs in about one in 5,000 to 7,000 live births.

Does trisomy 18 run in families?

Trisomy 18 is caused by and extra chromosome 18 being present in either the egg or sperm that made the baby. This condition occurs sporadically, meaning parents cannot cause it to happen. Trisomy 18 does not typically run in families.

The ICD code Q913 is used to code Edwards syndrome

Edwards syndrome (also known as trisomy 18 [T18]) is a chromosomal abnormality caused by the presence of all, or part of, an extra 18th chromosome. This genetic condition almost always results from nondisjunction during meiosis. It is named after John Hilton Edwards, who first described the syndrome in 1960.

ICD-10-CM Alphabetical Index References for 'Q91.3 - Trisomy 18, unspecified'

The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code Q91.3. 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 Q91.3 and a single ICD9 code, 758.2 is an approximate match for comparison and conversion purposes.

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