icd 10 code for goldenhar syndrome

What is the ICD 10 Index for Goldenhar-Gorlin syndrome?

"Goldenhar (-Gorlin) syndrome" References in the ICD-10-CM Index to Diseases and Injuries References in the ICD-10-CM Index to Diseases and Injuries applicable to the clinical term "goldenhar (-gorlin) syndrome" Goldenhar (-Gorlin) syndrome - Q87.0 Congenital malformation syndromes predominantly affecting facial appearance

What is the ICD 10 code for CONGEN malform syndromes?

Q87.0 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. Short description: Congen malform syndromes predom affecting facial appearance. The 2018/2019 edition of ICD-10-CM Q87.0 became effective on October 1, 2018.

What is the ICD 10 code for diagnosis Q87?

Q87.0 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2018/2019 edition of ICD-10-CM Q87.0 became effective on October 1, 2018. This is the American ICD-10-CM version of Q87.0 - other international versions of ICD-10 Q87.0 may differ.

What is congenital malformation syndromes predominantly affecting facial appearance?

0 for Congenital malformation syndromes predominantly affecting facial appearance is a medical classification as listed by WHO under the range - Congenital malformations, deformations and chromosomal abnormalities .

What is the ICD-10 code for Pierre Robin sequence?

The ICD-10 code for “Pierre Robin sequence” is the ICD-10-RCPCH adaptation code Q87. 08.

What is the ICD-10 code for Moebius syndrome?

0 - Congenital malformation syndromes predominantly affecting facial appearance.

What is the ICD-10 code for developmental delay?

Encounter for screening for global developmental delays (milestones) Z13. 42 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.

What is Goldenhar syndrome?

Goldenhar syndrome is a rare congenital condition characterized by abnormal development of the eye, ear and spine. Also known as oculo-auriculo-vertebral spectrum or OAV, Goldenhar syndrome was first documented in 1952 by Maurice Goldenhar, an ophthalmologist and general practitioner.

What is the difference between Pierre Robin syndrome and sequence?

Pierre Robin syndrome (PRS) — also called Pierre Robin sequence — is a condition in which your baby has a small jaw (micrognathia), a tongue that falls back toward the throat (glossoptosis) and upper airway obstruction. Infants with the condition also commonly have an opening in the roof of the mouth (cleft palate).

What is ICD-10 code for Charge Syndrome?

The 2022 edition of ICD-10-CM Q89. 8 became effective on October 1, 2021. This is the American ICD-10-CM version of Q89.

What is the ICD-10 code for plagiocephaly?

ICD-10 code Q67. 3 for Plagiocephaly is a medical classification as listed by WHO under the range - Congenital malformations, deformations and chromosomal abnormalities .

Which of the following conditions would be reported with Code Q65 81?

Terms in this set (25) Which of the following conditions would be reported with code Q65. 81? Imaging of the renal area reveals congenital left renal agenesis and right renal hypoplasia.

What is the ICD-10 code for neurodevelopmental disorder?

Mental, Behavioral and Neurodevelopmental disorders ICD-10-CM F89 is grouped within Diagnostic Related Group(s) (MS-DRG v39.0): 886 Behavioral and developmental disorders.

What is ICD-10 code F88?

Other disorders of psychological developmentICD-10 code: F88 Other disorders of psychological development.

How do you code developmental delays?

ICD-9-CM Diagnosis Code 315.9 : Unspecified delay in development.

What is a complex syndrome?

A complex syndrome characterized mainly by aural, oral, and mandibular developmental anomalies which may vary from mild to severe and frequently involve one side of the body . Vertebral anomalies, epibulbar epidermoids, mental retardation, and numerous other anomalies are frequently associated.

What is a rare congenital malformation characterized by micrognathia, posterior retraction of the

A rare congenital malformation characterized by micrognathia, posterior retraction of the tongue, and cleft palate. A rare syndrome that is inherited in an autosomal dominant or recessive pattern and caused by mutations in the myh3 gene. It is a severe form of arthrogryposis.

What is a congenital malformation characterized by?

Congenital malformation characterized by micrognathia, glossoptosis and cleft palate.

The ICD code Q870 is used to code Pierre Robin syndrome

Pierre Robin syndrome (abbreviated to PRS, and also known as Pierre Robin malformation, Pierre Robin anomaly or Pierre Robin anomalad) is a congenital condition of facial abnormalities in humans. PRS is a sequence, i.e. a chain of certain developmental malformations, one entailing the next.

Coding Notes for Q87.0 Info for medical coders on how to properly use this ICD-10 code

Inclusion Terms are a list of concepts for which a specific code is used. The list of Inclusion Terms is useful for determining the correct code in some cases, but the list is not necessarily exhaustive.

MS-DRG Mapping

DRG Group #564-566 - Other musculoskeletal system and connective tissue diagnoses with MCC.

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. Click on any term below to browse the alphabetical index.

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 Q87.0 and a single ICD9 code, 756.0 is an approximate match for comparison and conversion purposes.