Related Conditions
Aland eye disease and ocular albinism(child)
X-linked ocular albinism, Nettleship type(child)
Autosomal recessive ocular albinism(child)
Ocular albinism with late-onset sensorineural deafness(child)
Albinism(parent)
Congenital anomaly of eye(parent)
Hereditary disorder of the visual system(parent)
Lesion of eye(parent)
Quick Facts
- SNOMED CT
- 26399002
- UMLS CUI
- C0078917
- Fully Specified Name
- Ocular albinism (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
Medical Disclaimer
This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.
Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.