icd 10 code for optic atrophy

What is the prognosis of optic atrophy?

Oct 01, 2021 · 2022 ICD-10-CM Diagnosis Code H47.2 Optic atrophy 2016 2017 2018 2019 2020 2021 2022 Non-Billable/Non-Specific Code H47.2 should not be used for reimbursement purposes as there are multiple codes below it that contain a greater level of detail. The 2022 edition of ICD-10-CM H47.2 became effective on October 1, 2021.

What causes optic atrophy?

Oct 01, 2021 · 2022 ICD-10-CM Diagnosis Code H47.219 Primary optic atrophy, unspecified eye 2016 2017 2018 2019 2020 2021 2022 Billable/Specific Code H47.219 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 H47.219 became effective on October 1, 2021.

What are the differential diagnoses for optic atrophy?

Oct 01, 2021 · Other optic atrophy, bilateral 2016 2017 2018 2019 2020 2021 2022 Billable/Specific Code H47.293 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 H47.293 became effective on October 1, 2021.

How is optic atrophy treated?

ICD-10-CM Code H47.2 Optic atrophy NON-BILLABLE | ICD-10 from 2011 - 2016 ICD Code H47.2 is a non-billable code. To code a diagnosis of this type, you must use one of the five child codes of H47.2 that describes the diagnosis 'optic atrophy' in more detail. H47.2 Optic atrophy H47.20 Unspecified optic atrophy H47.21 Primary optic atrophy

What is the ICD code for optic atrophy?

ICD Code H47.2 is a non-billable code. To code a diagnosis of this type, you must use one of the five child codes of H47.2 that describes the diagnosis 'optic atrophy' in more detail.

How does Leber's optic atrophy affect men?

Leber’s hereditary optic neuropathy (LHON) or Leber optic atrophy is a mitochondrially inherited (transmitted from mother to offspring) degeneration of retinal ganglion cells (RGCs) and their axons that leads to an acute or subacute loss of central vision; this affects predominantly young adult males. However, LHON is only transmitted through the mother as it is primarily due to mutations in the mitochondrial (not nuclear) genome and only the egg contributes mitochondria to the embryo. LHON is usually due to one of three pathogenic mitochondrial DNA (mtDNA) point mutations. These mutations are at nucleotide positions 11778 G to A, 3460 G to A and 14484 T to C, respectively in the ND4, ND1 and ND6 subunit genes of complex I of the oxidative phosphorylation chain in mitochondria. Men cannot pass on the disease to their offspring.

What is the ICD code for acute care?

Use a child code to capture more detail. ICD Code H47.2 is a non-billable code.

What is optic atrophy?

OPTIC ATROPHY-. atrophy of the optic disk which may be congenital or acquired. this condition indicates a deficiency in the number of nerve fibers which arise in the retina and converge to form the optic disk; optic nerve; optic chiasm; and optic tracts. glaucoma; ischemia; inflammation a chronic elevation of intracranial pressure toxins optic nerve compression and inherited conditions see optic atrophies hereditary are relatively common causes of this condition.#N#OPTIC ATROPHIES HEREDITARY-. hereditary conditions that feature progressive visual loss in association with optic atrophy. relatively common forms include autosomal dominant optic atrophy optic atrophy autosomal dominant and leber hereditary optic atrophy optic atrophy hereditary leber.#N#OPTIC ATROPHY AUTOSOMAL DOMINANT-. dominant optic atrophy is a hereditary optic neuropathy causing decreased visual acuity color vision deficits a centrocecal scotoma and optic nerve pallor hum. genet. 1998; 102: 79 86. mutations leading to this condition have been mapped to the opa1 gene at chromosome 3q28 q29. opa1 codes for a dynamin related gtpase that localizes to mitochondria.#N#OPTIC ATROPHY HEREDITARY LEBER-. a maternally linked genetic disorder that presents in mid life as acute or subacute central vision loss leading to central scotoma and blindness. the disease has been associated with missense mutations in the mtdna in genes for complex i iii and iv polypeptides that can act autonomously or in association with each other to cause the disease. from online mendelian inheritance in man http://www.ncbi.nlm.nih.gov/omim/ mim#535000 april 17 2001

What is dominant optic atrophy?

OPTIC ATROPHY AUTOSOMAL DOMINANT-. dominant optic atrophy is a hereditary optic neuropathy causing decreased visual acuity color vision deficits a centrocecal scotoma and optic nerve pallor hum. genet. 1998; 102: 79 86. mutations leading to this condition have been mapped to the opa1 gene at chromosome 3q28 q29. opa1 codes for a dynamin related gtpase that localizes to mitochondria.

What nerves are responsible for vision loss?

The optic nerve is a bundle of more than 1 million nerve fibers that carry visual messages. You have one connecting the back of each eye (your retina) to your brain. Damage to an optic nerve can cause vision loss. The type of vision loss and how severe it is depends on where the damage occurs. It may affect one or both eyes.

What causes optic neuritis?

Optic neuritis is an inflammation of the optic nerve. Causes include infections and immune-related illnesses such as multiple sclerosis. Sometimes the cause is unknown.

When was the ICd 10 code implemented?

FY 2016 - New Code, effective from 10/1/2015 through 9/30/2016 (First year ICD-10-CM implemented into the HIPAA code set)

Is H47.2 a valid code?

The code is not specific and is NOT valid for the year 2021 for the submission of HIPAA-covered transactions. Category or Header define the heading of a category of codes that may be further subdivided by the use of 4th, 5th, 6th or 7th characters.

What is the ICd 10 code for optic atrophy?

H47.20 is a billable diagnosis code used to specify a medical diagnosis of unspecified optic atrophy. The code H47.20 is valid during the fiscal year 2021 from October 01, 2020 through September 30, 2021 for the submission of HIPAA-covered transactions.#N#The ICD-10-CM code H47.20 might also be used to specify conditions or terms like atrophy of optic disc, atrophy of sector of optic disc, bilateral optic atrophy of eyes, complete optic atrophy, early onset cerebellar ataxia with retinitis pigmentosa and optic atrophy , optic atrophy, etc.#N#Unspecified diagnosis codes like H47.20 are acceptable when clinical information is unknown or not available about a particular condition. Although a more specific code is preferable, unspecified codes should be used when such codes most accurately reflect what is known about a patient's condition. Specific diagnosis codes should not be used if not supported by the patient's medical record.

What is optic atrophy?

OPTIC ATROPHY-. atrophy of the optic disk which may be congenital or acquired. this condition indicates a deficiency in the number of nerve fibers which arise in the retina and converge to form the optic disk; optic nerve; optic chiasm; and optic tracts. glaucoma; ischemia; inflammation a chronic elevation of intracranial pressure toxins optic nerve compression and inherited conditions see optic atrophies hereditary are relatively common causes of this condition.#N#OPTIC ATROPHIES HEREDITARY-. hereditary conditions that feature progressive visual loss in association with optic atrophy. relatively common forms include autosomal dominant optic atrophy optic atrophy autosomal dominant and leber hereditary optic atrophy optic atrophy hereditary leber.#N#OPTIC ATROPHY AUTOSOMAL DOMINANT-. dominant optic atrophy is a hereditary optic neuropathy causing decreased visual acuity color vision deficits a centrocecal scotoma and optic nerve pallor hum. genet. 1998; 102: 79 86. mutations leading to this condition have been mapped to the opa1 gene at chromosome 3q28 q29. opa1 codes for a dynamin related gtpase that localizes to mitochondria.#N#OPTIC ATROPHY HEREDITARY LEBER-. a maternally linked genetic disorder that presents in mid life as acute or subacute central vision loss leading to central scotoma and blindness. the disease has been associated with missense mutations in the mtdna in genes for complex i iii and iv polypeptides that can act autonomously or in association with each other to cause the disease. from online mendelian inheritance in man http://www.ncbi.nlm.nih.gov/omim/ mim#535000 april 17 2001

What is dominant optic atrophy?

OPTIC ATROPHY AUTOSOMAL DOMINANT-. dominant optic atrophy is a hereditary optic neuropathy causing decreased visual acuity color vision deficits a centrocecal scotoma and optic nerve pallor hum. genet. 1998; 102: 79 86. mutations leading to this condition have been mapped to the opa1 gene at chromosome 3q28 q29. opa1 codes for a dynamin related gtpase that localizes to mitochondria.

When was the ICd 10 code implemented?

FY 2016 - New Code, effective from 10/1/2015 through 9/30/2016 (First year ICD-10-CM implemented into the HIPAA code set)