Overview
Hereditary retinal dystrophy is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
Congenital stationary night blindness(child)
Cone dystrophy(child)
Rod dystrophy(child)
Retinal dystrophy in systemic lipidosis(child)
Retinitis pigmentosa(child)
Hyaline dystrophy of Bruch's membrane(child)
Vitreoretinal dystrophy(child)
Progressive cone-rod dystrophy(child)
Juvenile retinoschisis(child)
Hereditary retinal dystrophies in lipidoses(child)
Hyaline retinal dystrophy(child)
Hereditary macular dystrophy(child)
Hereditary retinal dystrophy primarily involving retinal pigment epithelium(child)
Hereditary retinal dystrophy primarily involving sensory retina(child)
Jalili syndrome(child)
Autosomal dominant vitreoretinochoroidopathy(child)
Retinitis punctata albescens(child)
Bothnia retinal dystrophy(child)
Intellectual disability, truncal obesity, retinal dystrophy and micropenis syndrome(child)
Severe early childhood onset retinal dystrophy(child)
Quick Facts
- SNOMED CT
- 41799005
- UMLS CUI
- C0154860
- Fully Specified Name
- Hereditary retinal dystrophy (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.