icd 10 code for peutz-jeghers syndrome

What is the ICD-10-CM index for Peutz-Jeghers disease or syndrome?

Oct 01, 2021 · Q85.8 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 Q85.8 became effective on October 1, 2021. This is the American ICD-10-CM version of Q85.8 - other international versions of ICD-10 Q85.8 may differ. Applicable To Peutz-Jeghers Syndrome

How many terms are in the parent term Peutz Jeghers disease or syndrome?

The ICD code Q858 is used to code Peutz-Jeghers syndrome Peutz-Jeghers syndrome, also known as hereditary intestinal polyposis syndrome, is an autosomal dominant genetic disease characterized by the development of benign hamartomatous polyps in the gastrointestinal tract and hyperpigmented macules on the lips and oral mucosa (melanosis).

What is the ICD 10 code for Dimitri-Sturge-Weber disease?

References in the ICD-10-CM Index to Diseases and Injuries applicable to the clinical term "peutz-jeghers disease or syndrome". Peutz-Jeghers disease or syndrome - Q85.8 Other phakomatoses, not elsewhere classified. Previous Term: Petrositis.

What is the ICD 10 code for phakomatosis?

There are 0 terms under the parent term 'Peutz Jeghers Disease Or Syndrome' in the ICD-10-CM Alphabetical Index. Peutz Jeghers Disease Or Syndrome See Code: Q85.8

What is Phakomatoses not elsewhere classified?

8 for Other phakomatoses, not elsewhere classified is a medical classification as listed by WHO under the range - Congenital malformations, deformations and chromosomal abnormalities .

What is the ICD 10 code for Sturge Weber syndrome?

Q85. 8 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 Q85. 8 became effective on October 1, 2021.

What is diagnosis code R63 8?

8: Other symptoms and signs concerning food and fluid intake.

What is diagnosis code z13?

Encounter for screening for other diseases and disordersScreening is the testing for disease or disease precursors in asymptomatic individuals so that early detection and treatment can be provided for those who test positive for the disease.

What is Weber Syndrome?

Weber syndrome, classically described as a midbrain stroke syndrome and superior alternating hemiplegia, involves oculomotor fascicles in the interpeduncular cisterns and cerebral peduncle, thereby causing ipsilateral third nerve palsy with contralateral hemiparesis.Feb 20, 2022

How is Sturge-Weber syndrome treated?

Treatment for Sturge-Weber syndrome is symptomatic. Laser treatment may be used to lighten or remove the birthmark. Anticonvulsant medications may be used to control seizures. Persons with drug-resistant seizures may be treated by surgical removal of epileptic brain tissue.Mar 27, 2019

What is the ICD-10 code for insomnia?

Code G47. 00 is the diagnosis code used for Insomnia, Unspecified, also known as Sleep state misperception (SSM). It is a sleep disorder characterized by difficulty in falling asleep and/or remaining asleep.

What is the ICD-10 for diarrhea?

ICD-10 | Diarrhea, unspecified (R19. 7)

What is the ICD-10-CM code for nausea and vomiting?

Nausea with vomiting, unspecified R11. 2 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 R11. 2 became effective on October 1, 2021.

What is the ICD-10 code for preventive care?

Preventive screenings 1, Screening hypertension; and V81. 2, Screening other and unspecified cardiovascular conditions, all crosswalk to ICD-10 code Z13. 6, Encounters for screening for cardiovascular disorders.

What is the ICD-10 code for medical screening exam?

ICD-10-CM Code for Encounter for general adult medical examination without abnormal findings Z00. 00.

What ICD-10 code covers CBC?

R68. 89 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.

The ICD code Q858 is used to code Peutz-Jeghers syndrome

Peutz-Jeghers syndrome, also known as hereditary intestinal polyposis syndrome, is an autosomal dominant genetic disease characterized by the development of benign hamartomatous polyps in the gastrointestinal tract and hyperpigmented macules on the lips and oral mucosa (melanosis).

Coding Notes for Q85.8 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 #826-830 - Myeloprolif disord or poorly differentiated neoplasms with major operating room procedure with MCC.

ICD-10-CM Alphabetical Index References for 'Q85.8 - Other phakomatoses, not elsewhere classified'

The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code Q85.8. 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 Q85.8 and a single ICD9 code, 759.6 is an approximate match for comparison and conversion purposes.