Oct 01, 2021 · M35.2 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. Short description: Behcet's disease The 2022 edition of ICD-10-CM M35.2 became effective on October 1, 2021. This is the American ICD-10-CM version of M35.2 - other international versions of ICD-10 M35.2 may differ.
M35.3 ICD-10-CM Code for Behcet's disease M35.2 ICD-10 code M35.2 for Behcet's disease is a medical classification as listed by WHO under the range - Diseases of the musculoskeletal system and connective tissue . Subscribe to Codify and get the code details in a flash. Request a Demo 14 Day Free Trial Buy Now Official Long Descriptor
Behcet's disease BILLABLE | ICD-10 from 2011 - 2016 M35.2 is a billable ICD code used to specify a diagnosis of behcet's disease. A 'billable code' is detailed enough to be used to specify a medical diagnosis. The ICD code M352 is used to code Behçet's disease
Oct 01, 2021 · M35.2 is a valid billable ICD-10 diagnosis code for Behcet's disease. It is found in the 2022 version of the ICD-10 Clinical Modification (CM) and can be used in all HIPAA-covered transactions from Oct 01, 2021 - Sep 30, 2022 .
M35.2 is a billable ICD code used to specify a diagnosis of behcet's disease. A 'billable code' is detailed enough to be used to specify a medical diagnosis.
Behçet's disease (BD) was named in 1937 after the Turkish dermatologist Hulusi Behçet, who first described the triple-symptom complex of recurrent oral aphthous ulcers, genital ulcers, and uveitis.
Behçet's disease or Behçet disease (/bɛˈtʃɛt/), sometimes called Behçet's syndrome, Morbus Behçet, Behçet-Adamantiades syndrome, or Silk Road disease, is a rare immune-mediated small-vessel systemic vasculitis that often presents with mucous membrane ulceration and ocular problems. Behçet's disease (BD) was named in 1937 after the Turkish dermatologist Hulusi Behçet, who first described the triple-symptom complex of recurrent oral aphthous ulcers, genital ulcers, and uveitis. As a systemic disease, it can also involve visceral organs such as the gastrointestinal tract, pulmonary, musculoskeletal, cardiovascular and neurological systems. This syndrome can be fatal due to ruptured vascular aneurysms or severe neurological complications.
This inflammation most commonly affects small blood vessels in the mouth, genitals, skin, and eyes.Painful mouth sores called aphthous ulcers are usually the first sign of Behçet disease.
It mainly affects people in their 20s and 30s. Diagnosing Behcet's can take a long time, because symptoms may come and go, and it may take months or even years to have all of the symptoms. There is no cure.
The ulcers look like common canker sores, and they typically heal within one to two weeks. About 75 percent of all people with Behçet disease develop similar ulcers on the genitals.
Behcet's Syndrome. Also called: Behcet's disease . Behcet's syndrome is a disease that involves vasculitis, which is inflammation of the blood vessels. It causes problems in many parts of the body. The most common symptoms are. Sores in the mouth. Sores on the sex organs. Other skin sores. Swelling of parts of the eye.
Pain, swelling and stiffness of the joints. More serious problems can include meningitis, blood clots, inflammation of the digestive system and blindness. Doctors aren't sure what causes Behcet's. It is rare in the United States, but is common in the Middle East and Asia.
Valid for Submission. M35.2 is a billable diagnosis code used to specify a medical diagnosis of behcet's disease. The code M35.2 is valid during the fiscal year 2021 from October 01, 2020 through September 30, 2021 for the submission of HIPAA-covered transactions.
Involvement of the gastrointestinal tract can lead to a hole in the wall of the intestine (intestinal perforation), which can cause serious infection and may be life-threatening.The signs and symptoms of Behçet disease usually begin in a person's twenties or thirties, although they can appear at any age.