Hereditary optic atrophy
ICD-10 Code
H47.22
Hereditary optic atrophy
Definition
A family of inherited disorders characterized by progressive loss of vision secondary to death of the retinal ganglion cell axons that comprise the optic nerve.
Also known as hereditary optic atrophy — per MONDO
Also identified as
- ICD10CM H47.22 per MONDO
- MESH D015418 per MONDO
- NCIT C34864 per MONDO
- SCTID 26360005 per MONDO
- UMLS C0029125 per MONDO
Affected Organs
| Organ | Involvement | Source |
|---|---|---|
| Camera-type eye | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Camera-type eye | Disease Has Primary Anatomic Site | NCIT · CC BY 4.0 |