National Center for Advancing and Translational Sciences Genetic and Rare Diseases Information Center, a program of the National Center for Advancing and Translational Sciences

Familial partial lipodystrophy associated with PPARG mutations



Other Names:
Familial partial lipodystrophy type 3; FPLD3; LIPODYSTROPHY, FAMILIAL PARTIAL, ASSOCIATED WITH PPARG MUTATIONS; Familial partial lipodystrophy type 3; FPLD3; LIPODYSTROPHY, FAMILIAL PARTIAL, ASSOCIATED WITH PPARG MUTATIONS; PPARG-related familial partial lipodystrophy; PPARG-related FPLD See More
Categories:
This disease is grouped under:

This table lists symptoms that people with this disease may have. For most diseases, symptoms will vary from person to person. People with the same disease may not have all the symptoms listed. This information comes from a database called the Human Phenotype Ontology (HPO) . The HPO collects information on symptoms that have been described in medical resources. The HPO is updated regularly. Use the HPO ID to access more in-depth information about a symptom.

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Medical Terms Other Names
Learn More:
HPO ID
100% of people have these symptoms
Hypertension 0000822
Lipoatrophy
Loss of fat tissue in localized area
0100578
80%-99% of people have these symptoms
Hepatomegaly
Enlarged liver
0002240
Hypertriglyceridemia
Increased plasma triglycerides
Increased serum triglycerides
Increased triglycerides
[ more ]
0002155
Insulin-resistant diabetes mellitus
Insulin resistant diabetes
Insulin-resistant diabetes
[ more ]
0000831
Loss of subcutaneous adipose tissue in limbs
Loss of fat tissue below the skin in limbs
0003635
Xanthomatosis
Yellow bumps of fatty deposits on skin
0000991
30%-79% of people have these symptoms
Marked muscular hypertrophy 0009042
Secondary amenorrhea
Previous menstrual periods stop
0000869
Thin skin 0000963
5%-29% of people have these symptoms
Abnormality of skeletal muscle fiber size 0012084
Acanthosis nigricans
Darkened and thickened skin
0000956
Calf muscle pseudohypertrophy 0003707
Congestive heart failure
Cardiac failure
Cardiac failures
Heart failure
[ more ]
0001635
Coronary artery atherosclerosis
Plaque build-up in arteries supplying blood to heart
0001677
Dysmenorrhea
Painful menstruation
0100607
Eclampsia 0100601
Generalized hirsutism
Excessive hairiness over body
0002230
Hepatic steatosis
Fatty infiltration of liver
Fatty liver
[ more ]
0001397
Hypertrophic cardiomyopathy
Enlarged and thickened heart muscle
0001639
Hyperuricemia
High blood uric acid level
0002149
Loss of facial adipose tissue
Decreased amount of facial fat
Loss of facial fat
[ more ]
0000292
Maternal diabetes
gestational diabetes
0009800
Myalgia
Muscle ache
Muscle pain
[ more ]
0003326
Myopathy
Muscle tissue disease
0003198
Oligomenorrhea
Light or infrequent menstrual periods
0000876
Pancreatitis
Pancreatic inflammation
0001733
Polycystic ovaries 0000147
Splenomegaly
Increased spleen size
0001744
1%-4% of people have these symptoms
Cirrhosis
Scar tissue replaces healthy tissue in the liver
0001394
Primary amenorrhea 0000786
Prominent veins on trunk 0007457
Percent of people who have these symptoms is not available through HPO
Abnormality of the face
Abnormal face
Facial abnormality
[ more ]
0000271
Abnormality of the musculature
Muscular abnormality
0003011
Abnormality of the neck 0000464
Autosomal dominant inheritance 0000006
Decreased HDL cholesterol concentration
Decreased circulating high-density lipoprotein cholesterol
Decreased HDL cholesterol
Low HDL-cholesterol
[ more ]
0003233
Hirsutism
Excessive hairiness
0001007
Hyperglycemia
High blood sugar
0003074
Hyperinsulinemia 0000842
Lipodystrophy
Inability to make and keep healthy fat tissue
0009125
Loss of gluteal subcutaneous adipose tissue
Loss of fat tissue below the skin in gluts
0009017
Preeclampsia 0100602
Prominent superficial veins
Prominent veins
0001015
Reduced subcutaneous adipose tissue
Reduced fat tissue below the skin
0003758
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Last updated: 7/1/2020

If you need medical advice, you can look for doctors or other healthcare professionals who have experience with this disease. You may find these specialists through advocacy organizations, clinical trials, or articles published in medical journals. You may also want to contact a university or tertiary medical center in your area, because these centers tend to see more complex cases and have the latest technology and treatments.

If you can’t find a specialist in your local area, try contacting national or international specialists. They may be able to refer you to someone they know through conferences or research efforts. Some specialists may be willing to consult with you or your local doctors over the phone or by email if you can't travel to them for care.

You can find more tips in our guide, How to Find a Disease Specialist. We also encourage you to explore the rest of this page to find resources that can help you find specialists.

Healthcare Resources


These resources provide more information about this condition or associated symptoms. The in-depth resources contain medical and scientific language that may be hard to understand. You may want to review these resources with a medical professional.

Where to Start

  • Genetics Home Reference (GHR) contains information on Familial partial lipodystrophy associated with PPARG mutations. This website is maintained by the National Library of Medicine.

In-Depth Information

  • The Monarch Initiative brings together data about this condition from humans and other species to help physicians and biomedical researchers. Monarch’s tools are designed to make it easier to compare the signs and symptoms (phenotypes) of different diseases and discover common features. This initiative is a collaboration between several academic institutions across the world and is funded by the National Institutes of Health. Visit the website to explore the biology of this condition.
  • Online Mendelian Inheritance in Man (OMIM) is a catalog of human genes and genetic disorders. Each entry has a summary of related medical articles. It is meant for health care professionals and researchers. OMIM is maintained by Johns Hopkins University School of Medicine. 
  • Orphanet is a European reference portal for information on rare diseases and orphan drugs. Access to this database is free of charge.

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