Inherited retinal dystrophy
ICD-10 Code
H35.5
Inherited retinal dystrophy
Definition
An instance of retinal degeneration that is caused by an inherited modification of the individual's genome.
Also known as familial retinal dystrophy, genetic retinal dystrophy, hereditary retinal degeneration, hereditary retinal dystrophy, inherited retinal dystrophy, retinal dystrophy — per MONDO
Also identified as
- DOID 8500 per MONDO
- DOID 8501 per MONDO
- ICD10CM H35.5 per MONDO
- ICD9 362.7 per MONDO
- ICD9 362.70 per MONDO
- ICD9 362.72 per MONDO
- ICD9 362.75 per MONDO
- MESH D058499 per MONDO
- NCIT C35194 per MONDO
- NCIT C35625 per MONDO
- Orphanet 71862 per MONDO
- SCTID 314407005 per MONDO
- SCTID 41799005 per MONDO
- UMLS C0854723 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 |
| Retina | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Retina | Disease Has Primary Anatomic Site | NCIT · CC BY 4.0 |