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ICD-10-CM Code H47.22
Hereditary optic atrophy

BILLABLE
Billable Code
Billable codes are sufficient justification for admission to an acute care hospital when used a principal diagnosis.
| ICD-10 from 2011 - 2016

H47.22 is a billable ICD code used to specify a diagnosis of hereditary optic atrophy. A 'billable code' is detailed enough to be used to specify a medical diagnosis.


The ICD code H472 is used to code Leber's hereditary optic neuropathy

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.

Specialty: Ophthalmology
MeSH Code: D029242
ICD 9 Code: 377.16
Source: Wikipedia

Coding Notes for H47.22 Info for medical coders on how to properly use this ICD-10 code

Inclusion Terms:
Inclusion Terms
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.
Leber's optic atrophy

MS-DRG Mapping

  • DRG Group #123 - Neurological eye disorders.

ICD-10-CM Alphabetical Index References for 'H47.22 - Hereditary optic atrophy'

The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code H47.22. Click on any term below to browse the alphabetical index.

Equivalent ICD-9 Code GENERAL EQUIVALENCE MAPPINGS (GEM)

Hereditary optic atrophy (exact match)

This is the official exact match mapping between ICD9 and ICD10, as provided by the General Equivalency mapping crosswalk. This means that in all cases where the ICD9 code 377.16 was previously used, H47.22 is the appropriate modern ICD10 code.


Parent Code: H47.2 - Optic atrophy

** This Document Provided By ICD.Codes **
Source: http://icd.codes/icd10cm/H4722