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Retinitis pigmentosa, deafness, premature aging, short stature, facial dysmorphism syndrome
disorderSNOMED 1172605003CUI C5567466
Overview
Retinitis pigmentosa, deafness, premature aging, short stature, facial dysmorphism syndrome is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
Autosomal recessive retinitis pigmentosa(parent)
Multiple malformation syndrome with facial-limb defects as major feature(parent)
Disorder of stature(parent)
Developmental hereditary disorder(parent)
Premature ageing syndrome(parent)
Brachydactyly(parent)
Sensorineural hearing loss(parent)
Hereditary hearing loss(parent)
Quick Facts
- SNOMED CT
- 1172605003
- UMLS CUI
- C5567466
- Fully Specified Name
- Retinitis pigmentosa, hearing loss, premature aging, short stature, facial dysmorphism 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.