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Muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus
disorderSNOMED 237611007CUI C0342281
Overview
Muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Ataxia
HP:0001251
Diabetes mellitus
HP:0000819
Muscle atrophy, neurogenic
HP:0003202
Rod-cone dystrophy
HP:0000510
Related Conditions
Amyotrophia(parent)
Autosomal dominant hereditary disorder(parent)
Hereditary disorder of endocrine system(parent)
Hereditary disorder of musculoskeletal system(parent)
Hereditary disorder of the visual system(parent)
Diabetes mellitus associated with genetic syndrome(parent)
Hereditary ataxia(parent)
Degeneration of retina(parent)
Quick Facts
- SNOMED CT
- 237611007
- UMLS CUI
- C0342281
- Fully Specified Name
- Muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 4
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.