Clinical Trials
1
Total Trials
1
Recruiting
0
With Results
Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Atrophy of fat
Very frequent (80-99%)HP:0100578
Autoimmunity
Frequent (30-79%)HP:0002960
Decreased serum complement C3 level
Frequent (30-79%)HP:0005421
Epilepsy
Frequent (30-79%)HP:0001250
Hearing impairment
Frequent (30-79%)HP:0000365
Increased total lymphocyte count
Frequent (30-79%)HP:0100827
Mental-retardation
Frequent (30-79%)HP:0001249
Myopathy
Frequent (30-79%)HP:0003198
Progeroid facial appearance
Frequent (30-79%)HP:0005328
Arthritic pain
Occasional (5-29%)HP:0002829
Body fails to respond to insulin
Occasional (5-29%)HP:0000855
Fatty liver
Occasional (5-29%)HP:0001397
Generalized hirsutism
Occasional (5-29%)HP:0002230
Glomerulopathy
Occasional (5-29%)HP:0100820
Immune deficiency
Occasional (5-29%)HP:0002721
Microhematuria
Occasional (5-29%)HP:0002907
Proteinuria
Occasional (5-29%)HP:0000093
Quick Facts
- SNOMED CT
- 75659004
- UMLS CUI
- C0220989
- Fully Specified Name
- Acquired partial lipodystrophy (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 17
- 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.