Related Conditions
Choroideremia with deafness and obesity syndrome(child)
Alport syndrome X-linked(child)
Abruzzo Erickson syndrome(child)
Deafness and intellectual disability Martin Probst type syndrome(child)
Ocular albinism with late-onset sensorineural deafness(child)
Sensorineural hearing loss(parent)
X-linked hereditary disease(parent)
Hereditary hearing loss(parent)
Quick Facts
- SNOMED CT
- 232329002
- UMLS CUI
- C0395972
- Fully Specified Name
- X-linked sensorineural hearing loss (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.