Concept ID: 724207001 Read Codes: XaYYN ICD-10 Codes: Q878 Powered by X-Lab. ICD-9-CM 726.2 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, 726.2 should only be used for claims with a date of service on or before September 30, 2015. Short description: Microdeletions NEC. Valid for Submission.
This code is grouped under diagnosis codes for congenital malformations, deformations and chromosomal abnormalities. The code is valid for the year 2020 for the submission of HIPAA-covered transactions. Russell-Silver syndrome (RSS) is a rare congenital condition.
For claims with a date of service on or after October 1, 2015, use an equivalent ICD-10-CM code (or codes). - Kleefstra syndrome (disorder) - Kleefstra syndrome Hide descriptions.
Short description: Shoulder region dis NEC. Most symptoms can be treated.
It does not include a difference of one or more complete sets of chromosomes.A cell with any number of complete chromosome sets is called a euploid cell.. An extra or missing chromosome is a common cause of some genetic disorders. Om icd.nu Kontakta icd.nu Sökalternativ Användarkonton Primärvård Tillägg (plugin) Diagnoslistor Om kliniklistor Snabblistan Kalkylatorerna Kommentarer Asterisk- / daggerpar Webapp E D For claims with a date of service on or after October 1, 2015, use an equivalent ICD-10-CM code (or codes).
Q98.4 is a billable code used to specify a medical diagnosis of klinefelter syndrome, unspecified. Click on any term below to browse the alphabetical index. Aneuploidy is the presence of an abnormal number of chromosomes in a cell, for example a human cell having 45 or 47 chromosomes instead of the usual 46. This tool allows you to search SNOMED CT and is designed for educational use only. ADNP syndrome occurs most frequently as a new (sporadic or de novo) mutation, which means that in most reported patients, the gene mutation has occurred at the time of the formation of the egg or sperm/during embryonic development for that child only, and no other family member will be affected. See more ideas about Syndrome, Rare genetic disorders, Hypotonia. ICD-9-CM 758.33 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, 758.33 should only be used for claims with a date of service on or before September 30, 2015. May 19, 2015 - Explore snowballs2's board "Kleefstra Syndrome", followed by 129 people on Pinterest. ICD-10 Q87.89 is other specified congenital malformation syndromes, not elsewhere classified (Q8789). Sindromul Kleefstra este un sindrom rar și relativ nou ce a fost descoperit de către Dr. Tjitske Kleefstra în anul 2006.
The features of 9q34 duplication do occur in this way, so the disorder is known as 9q34 duplication syndrome. It is characterized by stunted growth and limb or facial asymmetry. ICD-10-CM Alphabetical Index References for 'Q87.0 - Congenital malformation syndromes predominantly affecting facial appearance' The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code Q87.0. Oficial au fost raportate aproximativ 500 de cazuri, dar este posibil ca sindromul să fie subdiagnosticat. The ICD-10-CM code Q98.4 might also be used to specify conditions or terms like klinefelter syndrome. 9q34 duplication syndrome When a particular set of developmental features occurs in a recognisable and consistent pattern in enough people, as a result of a single cause, the condition is called a syndrome.