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Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome
disorderSNOMED 778021002CUI C4755272
Overview
Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
Microphthalmos(parent)
Autosomal recessive retinitis pigmentosa(parent)
Inherited optic neuropathy(parent)
Hereditary degenerative disease of central nervous system(parent)
Optic disk disorder(parent)
Developmental hereditary disorder(parent)
Retinoschisis(parent)
Abnormality of fovea centralis morphology(parent)
Abnormality of fundus of eye morphology(parent)
Quick Facts
- SNOMED CT
- 778021002
- UMLS CUI
- C4755272
- Fully Specified Name
- Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome (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.