Related Conditions
Oculotrichodysplasia(child)
Spastic tetraplegia, retinitis pigmentosa, intellectual disability syndrome(child)
Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome(child)
Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome(child)
Autosomal recessive posterior column ataxia and retinitis pigmentosa(child)
Cleft lip retinopathy syndrome(child)
Retinitis pigmentosa-deafness syndrome(child)
Autosomal recessive leukoencephalopathy, ischemic stroke, retinitis pigmentosa syndrome(child)
Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome(child)
RHYNS syndrome(child)
Retinitis pigmentosa, deafness, premature aging, short stature, facial dysmorphism syndrome(child)
Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome(child)
PXE-like (pseudoxanthoma elasticum-like) syndrome with retinitis pigmentosa(child)
Retinitis pigmentosa(parent)
Recessive hereditary disorder (autosomal)(parent)
Quick Facts
- SNOMED CT
- 232053004
- UMLS CUI
- C0339526
- Fully Specified Name
- Autosomal recessive retinitis pigmentosa (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.