Clinical Trials
1
Total Trials
0
Recruiting
0
With Results
Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Acanthosis nigricans
HP:0000956
Related Conditions
Acanthosis nigricans of oral mucous membranes(child)
Crouzon syndrome with acanthosis nigricans(child)
Acanthosis nigricans and insulin resistance with muscle cramp and acral enlargement syndrome(child)
Lelis syndrome(child)
Acquired acanthosis nigricans(child)
Severe achondroplasia, developmental delay, acanthosis nigricans syndrome(child)
Cutis gyrata syndrome of Beare and Stevenson(child)
Malignant acanthosis nigricans(child)
Disorder of keratinisation(parent)
Quick Facts
- SNOMED CT
- 402599005
- UMLS CUI
- C0000889
- Fully Specified Name
- Acanthosis nigricans (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 1
- Clinical Trials
- 1
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.