icd 9 code for ehlers-danlos syndrome eye code

What is the ICD 10 code for Ehlers Danlos syndrome?

Ehlers-Danlos syndrome. Q79.6 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2019 edition of ICD-10-CM Q79.6 became effective on October 1, 2018. This is the American ICD-10-CM version of Q79.6 - other international versions of ICD-10 Q79.6 may differ.

What is Ehlers-Danlos syndrome (EDS)?

Ehlers-danlos syndrome (eds) is a group of inherited disorders that weaken connective tissues. Connective tissues are proteins that support skin, bones, blood vessels and other organs. Eds usually affects your skin, joints and blood vessel walls. Symptoms include there are several types of eds.

How does Ehlers Danlos syndrome affect the body?

Ehlers-danlos syndrome (eds) is a group of inherited disorders that weaken connective tissues. Connective tissues are proteins that support skin, bones, blood vessels and other organs. Eds usually affects your skin, joints and blood vessel walls. Symptoms include loose joints. fragile, small blood vessels.

What is the diagnosis code for Ehlers-Danlos syndrome?

ICD-10 code Q79. 6 for Ehlers-Danlos syndromes is a medical classification as listed by WHO under the range - Congenital malformations, deformations and chromosomal abnormalities .

Does Ehlers-Danlos syndrome affect the eyes?

Ehlers Danlos Syndrome patients are prone to myopia and elongated eyes due to the stretching of the collagenous sclera.

What is Ehlers-Danlos syndrome unspecified?

Ehlers-Danlos syndrome is a group of inherited disorders that affect your connective tissues — primarily your skin, joints and blood vessel walls. Connective tissue is a complex mixture of proteins and other substances that provide strength and elasticity to the underlying structures in your body.

Is Ehlers-Danlos syndrome degenerative?

EDS is a progressive, degenerative connective tissue disorder that causes microtears in multiple organs. It is common to see EDS patients entering their teens or twenties who then develop severe pain.

Can hypermobility syndrome affect your eyes?

Conclusions: The most consistent association of eye anomalies in the JHS/EDS-HT group included xerophthalmia, steeper corneas, pathologic myopia, and vitreous abnormalities, as well as a higher rate of minor lens opacities.

Does Ehlers-Danlos cause dry eyes?

Dry eye may be the most common of these eye-related concerns, affecting 63% of patients; this manifests in those with EDS mostly as a result of impaired blinking processes and/or closure of the eyelids, thus resulting in inflamed eyes caused by over-exposure to the environment.

What are the 14 types of Ehlers-Danlos?

Types of Ehlers-Danlos SyndromeArthrochalasia EDS. ... Brittle Cornea Syndrome. ... Cardiac-Valvular EDS. ... Classical EDS. ... Classical-like EDS. ... Dermatosparaxis EDS. ... Hypermobile EDS. ... Kyphoscoliotic EDS.More items...

Is Ehlers-Danlos syndrome an autoimmune disease?

In the United States, two million people live with rheumatoid arthritis, and another 1.5 million live with lupus. A much rarer group of connective tissue disorders is called Ehlers-Danlos syndrome. Unlike the diseases noted above, Ehlers-Danlos syndrome is not an autoimmune condition, it's an inherited disorder.

What are the different types of Ehlers-Danlos syndrome?

2017 International Diagnostic CriteraEDS Types Chart.Classical EDS (cEDS)Classical-like EDS (clEDS)Cardiac-valvular EDS (cvEDS)Vascular EDS (vEDS)Hypermobile EDS.Arthrochalasia EDS (aEDS)Dermatosparaxis EDS (dEDS)More items...

Is Ehlers-Danlos syndrome a disability?

Applying for Social Security Disability with Ehlers-Danlos Syndrome. Like many rare genetic conditions, there is no Blue Book listing for Ehlers-Danlos. However, you may still qualify for benefits if you can match a listing associated with your particular symptoms or impairments.

Is rheumatoid arthritis related to Ehlers-Danlos syndrome?

There is about one case of Ehlers-Danlos for every 50 with rheumatoid arthritis or every five people with lupus. Features common to most of the 13 include very mobile joints that dislocate easily, skin that you see through, poor wound healing with a specific type of scars.

Is Ehlers-Danlos a neurological disorder?

Ehlers–Danlos syndrome (EDS) is a heterogeneous heritable connective tissue disorder with various neurological manifestations, including chronic pain. The neurological manifestations in EDS are often regarded as being caused by the associated musculoskeletal disorders or polyneuropathy.

What is Ehlers Danlos syndrome?

Clinical Information. A heterogeneous group of autosomally inherited collagen diseases caused by defects in the synthesis or structure of fibrillar collagen. There are numerous subtypes: classical, hypermobility, vascular, and others.

What are the inherited disorders of the connective tissue?

Group of inherited disorders of the connective tissue; major manifestations include hyperextensible skin and joints, easy bruisability, friability of tissues with bleeding and poor wound healing, calcified subcutaneous spheroids, and pseudotumors. Code History.