← Back to Conditions

Acquired partial lipodystrophy

disorder
SNOMED 75659004CUI C0220989

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

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.