Trisomy 21, translocation
Q90. 2 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.How do you test for trisomy 21?
- Congenital heart disease
- Gastrointestinal abnormalities
- Musculoskeletal and movement problems
- Spine disorders such as scoliosis, kyphosis or lordosis
- Endocrinologic disorders
- Epilepsy
- Hearing loss
- Speech apraxia (difficulty making speech sounds)
- Sleep disorders
- Feeding disorders
What disease is caused by trisomy 21?
Down syndrome or Down's syndrome, also known as trisomy 21, is a genetic disorder caused by the presence of all or part of a third copy of chromosome 21. It is usually associated with physical growth delays, mild to moderate intellectual disability, and characteristic facial features.
What is high risk for trisomy 21?
The risk of trisomy 21 is directly related to maternal age. All forms of prenatal testing for Down syndrome must be voluntary. A nondirective approach should be used when presenting patients with options for prenatal screening and diagnostic testing.
Does trisomy 21 affect more males or females?
Male prevalence (an overall SR of 1.24) was found in children with all trisomy 21 variants except the cases with mosaicism (the ratio of 0.88). The most expressed male predominance was determined...
What is the ICD-10 code for congenital Trisomy 21 in the newborn?
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 diagnosis code for Trisomy 21?
Q90. 0 (Down syndrome, Trisomy 21, nonmosaicism)
What is the ICD-10 code for fetal abnormality?
ICD-10 code O35. 8XX0 for Maternal care for other (suspected) fetal abnormality and damage, not applicable or unspecified is a medical classification as listed by WHO under the range - Pregnancy, childbirth and the puerperium .
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 Trisomy 21 a disease?
Down syndrome is a genetic disorder. It is also called trisomy 21. It includes certain birth defects, learning problems, and facial features. A child with Down syndrome also may have heart defects and problems with vision and hearing.
What is the CPT code for Down syndrome?
Neuromuscular Re-education: 97112.
What is fetal cardiac anomaly?
Conotruncal anomalies are a category of cardiac abnormalities characterized by a defect in the conotruncal septum and include truncus arteriosus, malposition of the great arteries, tetralogy of Fallot, double-outlet right ventricle, and a ventricular septal defect with an overriding aorta.
What is suspected fetal anomaly?
An anomaly is something that is different from what is normal or expected. Fetal anomalies refer to unusual or unexpected conditions in a baby's development during pregnancy. Fetal anomalies may also be known as congenital anomalies or birth defects.
What is ICD-10 code for fetal intolerance of labor?
ICD-10 code O77. 9 for Labor and delivery complicated by fetal stress, unspecified is a medical classification as listed by WHO under the range - Pregnancy, childbirth and the puerperium .
What is the ICD-10 code for advanced maternal age?
O09. 521 is applicable to maternity patients aged 12 - 55 years inclusive.
What is the ICD-10 code for amniocentesis?
2022 ICD-10-CM Diagnosis Code Z36. 0: Encounter for antenatal screening for chromosomal anomalies.
What is the ICD-10 code for developmental delay?
315.9 - Unspecified delay in development | ICD-10-CM.
What is the term for the presence of a third copy of chromosome 21?
A chromosomal abnormality consisting of the presence of a third copy of chromosome 21 in somatic cells. A chromosomal dysgenesis syndrome resulting from a triplication or translocation of chromosome 21. Down syndrome occurs in approximately 1:700 live births.
What is the name of the syndrome that results from having an extra copy of chromosome 21?
Down syndrome is set of mental and physical symptoms that result from having an extra copy of chromosome 21. Even though people with down syndrome may have some physical and mental features in common, symptoms of down syndrome can range from mild to severe.
What is the risk of leukemia in Down syndrome?
Patients with down syndrome have an estimated 10 to 30-fold increased risk for leukemia; most have symptoms of alzheimer's disease by age 40. Also known as trisomy 21 syndrome. A chromosome disorder associated either with an extra chromosome 21 or an effective trisomy for chromosome 21.
MS-DRG Mapping
DRG Group #781 - Other antepartum diagnoses with medical complications.
Equivalent ICD-9 Codes 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 O35.1XX0 and a single ICD9 code, 655.13 is an approximate match for comparison and conversion purposes.
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